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ChemicalBook >> CAS DataBase List >>4-(N-Boc-amino)phenylboronic acid pinacol ester

4-(N-Boc-amino)phenylboronic acid pinacol ester

CAS No.
330793-01-6
Chemical Name:
4-(N-Boc-amino)phenylboronic acid pinacol ester
Synonyms
N-Boc-4-aminophenylboronic acid pinacol ester;4-BUT;SKL693;[4-(4,4,5;tert-Butyl-N-[4-(4;2-dioxaborolan-2-yl)phenyl]carbaMate;4-n-boc-phenylboronic acid pinacol ester;tert-Butyl-N-[4-(4,4,5,5-tetramethyl-1,3,2-;4-(Boc-aMino)benzenboronic acid pinacol ester;4-(BOC-AMINO)BENZENEBORONIC ACID PINACOL ESTER
CBNumber:
CB3686465
Molecular Formula:
C17H26BNO4
Molecular Weight:
319.2
MDL Number:
MFCD02179439
MOL File:
330793-01-6.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 04:25:03
Product description Number Pack Size Price
4-(N-Boc-amino)phenylboronic acid pinacol ester 97% 562351 1g $78.6
4-(N-Boc-amino)phenylboronic acid pinacol ester 97% 562351 5g $226
N-(tert-Butoxycarbonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline >99.0%(HPLC)(T) B5588 1g $34
N-(tert-Butoxycarbonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline >99.0%(HPLC)(T) B5588 5g $113
t-Butyl-N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamate, min. 97% min.97% 05-0360 1g $109
More product size

4-(N-Boc-amino)phenylboronic acid pinacol ester Properties

Melting point 167-170 °C(lit.)
Boiling point 381.1±25.0 °C(Predicted)
Density 1.07±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form Crystalline Powder
pka 14.00±0.70(Predicted)
color White to off-white
InChI InChI=1S/C17H26BNO4/c1-15(2,3)21-14(20)19-13-10-8-12(9-11-13)18-22-16(4,5)17(6,7)23-18/h8-11H,1-7H3,(H,19,20)
InChIKey HSJNIOYPTSKQBD-UHFFFAOYSA-N
SMILES C(OC(C)(C)C)(=O)NC1=CC=C(B2OC(C)(C)C(C)(C)O2)C=C1
CAS DataBase Reference 330793-01-6(CAS DataBase Reference)
UNSPSC Code 12352103
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
PPE Eyeshields, Gloves, type N95 (US)
Hazard Codes  Xi,Xn
Risk Statements  36/37/38-20/21/22-43
Safety Statements  37/39-26-36-36/37
WGK Germany  3
Hazard Note  Irritant
HS Code  29349990
Storage Class 11 - Combustible Solids
NFPA 704
0
2 0

4-(N-Boc-amino)phenylboronic acid pinacol ester price More Price(97)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 562351 4-(N-Boc-amino)phenylboronic acid pinacol ester 97% 330793-01-6 1g $78.6 2026-04-30 Buy
Sigma-Aldrich 562351 4-(N-Boc-amino)phenylboronic acid pinacol ester 97% 330793-01-6 5g $226 2026-04-30 Buy
TCI Chemical B5588 N-(tert-Butoxycarbonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline >99.0%(HPLC)(T) 330793-01-6 1g $34 2026-04-30 Buy
TCI Chemical B5588 N-(tert-Butoxycarbonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline >99.0%(HPLC)(T) 330793-01-6 5g $113 2026-04-30 Buy
Strem Chemicals 05-0360 t-Butyl-N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamate, min. 97% min.97% 330793-01-6 1g $109 2026-04-30 Buy
Product number Packaging Price Buy
562351 1g $78.6 Buy
562351 5g $226 Buy
B5588 1g $34 Buy
B5588 5g $113 Buy
05-0360 1g $109 Buy

4-(N-Boc-amino)phenylboronic acid pinacol ester Chemical Properties,Uses,Production

Chemical Properties

White crystalline powder

Uses

4-(Boc-amino)benzeneboronic acid pinacol ester is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

Synthesis

Bis(pinacolato)diboron

73183-34-3

TERT-BUTYL N-(4-BROMOPHENYL)-CARBAMATE

131818-17-2

4-(N-Boc-amino)phenylboronic acid pinacol ester

330793-01-6

Anhydrous dioxane (100 mL) was added to a 250 mL round-bottom flask using pinacol ester of bisboronic acid (10.5 g, 41.5 mmol) and N-tert-butoxycarbonyl-4-bromoaniline (7.75 g, 28.5 mmol). Pd(dppf)Cl2 (0.79 g, 1.1 mmol) and potassium acetate (7.0 g, 71.4 mmol) were subsequently added. The reaction mixture was stirred at 110 °C for 12 h under argon protection. After completion of the reaction, it was cooled to room temperature, filtered and the filtrate was concentrated by rotary evaporator. The residue was purified by silica gel column chromatography (eluent: petroleum ether/ethyl acetate, 10:1) to afford N-Boc-4-aminophenylboronic acid pinacol ester (3.26 g, 36% yield) as a white solid.1H NMR (400 MHz, DMSO-d6) δ 9.53 (s, 1H), 7.56 (d, J = 8.5 Hz, 2H), 7.47 (d, J = 8.5 Hz, 2H), 1.48 (s, 9H), 1.29 (s, 12H).

References

[1] Dyes and Pigments, 2017, vol. 137, p. 229 - 235
[2] Patent: US2002/156081, 2002, A1
[3] Patent: US6921763, 2005, B2
[4] Tetrahedron Letters, 2014, vol. 55, # 2, p. 305 - 309
[5] MedChemComm, 2014, vol. 5, # 10, p. 1507 - 1514

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View Lastest Price from 4-(N-Boc-amino)phenylboronic acid pinacol ester manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Carbamic acid, N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-, 1,1-dimethylethyl ester pictures 2026-04-17 Carbamic acid, N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-, 1,1-dimethylethyl ester
330793-01-6
$3.00-9.00 99% ZHENGZHOU JIUYI TIME NEW MATERIALS CO,.LTD
TERT-BUTYL-N-[4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL]CARBAMATE TERT-BUTYL-N-METHYL-N-[4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL]CARBAMATE N-BOC-N-METHYL-4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)ANILINE (4-BOC-N-METHYL-AMINOPHENYL)BORONIC ACID PINACOL ESTER 4-(BOC-AMINO)PHENYLBORONIC ACID PINACOL CYCLIC ESTER (4-BOC-AMINOPHENYL)BORONIC ACID, PINACOL ESTER 4-(BOC-AMINO)BENZENEBORONIC ACID PINACOL ESTER 4-BUTOXYCARBONYLAMINOPHENYLBORONIC ACID, PINACOL ESTER 4-(TERT-BUTOXYCARBONYL-N-METHYLAMINO)PHENYLBORONIC ACID, PINACOL ESTER 4-(TERT-BUTOXYCARBONYLAMINO)PHENYLBORONIC ACID, PINACOL ESTER 4-(T-BUTOXYCARBONYLAMINO)PHENYLBORONIC ACID, PINACOL ESTER 4-(Boc-amino)phenylboronic acid~4-(tert-Butoxycarbonylamino)benzeneboronic acid~4-(tert-Butoxycarbonylamino)phenylboronic acid Carbamic acid, N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-, 1,1-dimethylethyl ester tert-Butyl (4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl) 4-(N-Boc-amino)phenylboronic acid pinacol ester, 97% Carbamic acid, [4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-, 1,1-dimethylethyl ester (9CI) 4-(tert-Butoxycarbonylamino)benzeneboronicacid T-BUTYL-N-[4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL]CARBAMATE T-BUTYL N-[4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE-2-YL)PHENYL]CARBAMATE T-BUTYL-N-[(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL]CARBAMATE TERT-BUTYL-N-[4-(4,4,5,5-TETRAMETHYL-1,2,3-DIOXABOROLAN-2-YL)PHENYL]CARBAMATE 4-n-boc-phenylboronic acid pinacol ester tert-Butyl-N-[4-(4,4,5,5-tetramethyl-1,3,2- tert-Butyl-N-methyl-N-[4-(4,4,5,5-tetramethyl- 4-BUTOXYCARBONYLAMINOPHENYLBORONIC ACID, PINACOL 4-N-Boc-phenylboronic acid pinacol ester, tert-Butyl N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamate tert-Butyl-N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamate, 97+% t-Butyl-N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamate, min. 97% t-Butyl-N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamate,min.97% tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenylcarbamate 4-Aminobenzeneboronic acid, pinacol ester, N-BOC protected tert-Butyl [4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamate, 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline, N-BOC protected 4-(Boc-aMino)benzenboronic acid pinacol ester 2-dioxaborolan-2-yl)phenyl]carbaMate tert-Butyl-N-[4-(4 4-(N-Boc-amino)phenylboronic acid pinacol ester 97% tert-butyl N-[4-(tetraMethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbaMate N-(tert-Butoxycarbonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline 4-BUT t-Butyl N-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl) ert-butylN-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamate [4-(4,4,5 N-Boc-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline SKL693 4-(N-Boc-amino)phenylboronic acid pinacol ester tert-Butyl (4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate - [B1992] N-Boc-4-aminobenzeneboronic acid pinacol ester 4-(N-Boc-amino)phenylboronic acid pinacol ester N-Boc-4-aminophenylboronic acid pinacol ester 330793-01-6 C18H28BNO4 C11H26BNO4 C17H26BNO4 Organometallic Reagents Boronate Esters Boronic Acids and Derivatives Aryl organic or inorganic borate
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