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ChemicalBook >> CAS DataBase List >>tert-Butyl (1-(hydroxymethyl)cyclopropyl)carbamate

tert-Butyl (1-(hydroxymethyl)cyclopropyl)carbamate

CAS No.
107017-73-2
Chemical Name:
tert-Butyl (1-(hydroxymethyl)cyclopropyl)carbamate
Synonyms
tert-butyl N-[1-(hydroxymethyl)cyclopropyl]carbamate;N-BOC-1-AMINO-CYCLOPROPANEMETHANOL;tert-Butyl [1-(Hydroxymethyl)cyclopropyl]carbamate;SKL325;Boc-ACPC-ol;Boc-1-Amnocyclopropylmethanol;Boc-1-Aminocyclopropylmethanol;1-(Boc-amino)cyclopropylmethanol;N-Boc-1-AMinocyclopropylMethanol;Boc-1-aminocyclopropane methanol
CBNumber:
CB91508201
Molecular Formula:
C9H17NO3
Molecular Weight:
187.24
MDL Number:
MFCD09749954
MOL File:
107017-73-2.mol
MSDS File:
SDS
Last updated:2026-05-28 05:53:16
Product description Number Pack Size Price
[1-(tert-Butoxycarbonylamino)cyclopropyl]methanol >97.0%(GC) B4251 200mg $31
[1-(tert-Butoxycarbonylamino)cyclopropyl]methanol >97.0%(GC) B4251 1g $99
Boc-1-Aminocyclopropylmethanol 98% OR350017 1g $21
Boc-1-Aminocyclopropylmethanol 98% OR350017 5g $29
Boc-1-Aminocyclopropylmethanol 98% OR350017 10g $56
More product size

tert-Butyl (1-(hydroxymethyl)cyclopropyl)carbamate Properties

Melting point 81.0 to 85.0 °C
Boiling point 294.5±9.0 °C(Predicted)
Density 1.11±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form powder to crystal
pka 12.24±0.20(Predicted)
color White to Orange to Green
InChI InChI=1S/C9H17NO3/c1-8(2,3)13-7(12)10-9(6-11)4-5-9/h11H,4-6H2,1-3H3,(H,10,12)
InChIKey HFMAZNJKNNRONT-UHFFFAOYSA-N
SMILES C(OC(C)(C)C)(=O)NC1(CO)CC1

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H332-H335
Precautionary statements  P280-P305+P351+P338-P310
HS Code  2924297099

tert-Butyl (1-(hydroxymethyl)cyclopropyl)carbamate price More Price(95)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical B4251 [1-(tert-Butoxycarbonylamino)cyclopropyl]methanol >97.0%(GC) 107017-73-2 200mg $31 2026-04-30 Buy
TCI Chemical B4251 [1-(tert-Butoxycarbonylamino)cyclopropyl]methanol >97.0%(GC) 107017-73-2 1g $99 2026-04-30 Buy
Apolloscientific OR350017 Boc-1-Aminocyclopropylmethanol 98% 107017-73-2 1g $21 2026-06-04 Buy
Apolloscientific OR350017 Boc-1-Aminocyclopropylmethanol 98% 107017-73-2 5g $29 2026-06-04 Buy
Apolloscientific OR350017 Boc-1-Aminocyclopropylmethanol 98% 107017-73-2 10g $56 2026-06-04 Buy
Product number Packaging Price Buy
B4251 200mg $31 Buy
B4251 1g $99 Buy
OR350017 1g $21 Buy
OR350017 5g $29 Buy
OR350017 10g $56 Buy

tert-Butyl (1-(hydroxymethyl)cyclopropyl)carbamate Chemical Properties,Uses,Production

Physical Form

Solid

Uses

Tert-Butyl (1-(hydroxymethyl)cyclopropyl)carbamate could be converted into spirocyclopropanated analogues 14-CP and 14-CT of the insecticide Thiacloprid [1]. It can also be transformed into spirocyclopropanated analogs of Imidacloprid. This compound could be used to synthesize spirocyclopropanated five-membered ring analog 4-(3,5-Dichlorophenyl)-N-isopropyl-5-oxo-4,6-diazaspiro- [2.4]heptane-6-carboxamide[2].tert-Butyl (1-(hydroxymethyl)cyclopropyl)carbamate

Preparation

Tert-Butyl (1-(hydroxymethyl)cyclopropyl)carbamate can be synthesized in three steps (40 % overall yield) from N, Ndibenzyl-2-benzyloxyacetamide starting with its reductive cyclopropanation (the de Meijere variant of the so-called Kulinkovich reaction). It can also be prepared in 56 % overall yield by monohydrolysis of commercially available diethyl cyclopropane-1,1-dicarboxylate followed by Curtius degradation of the carboxylic acid residue and subsequent reduction of the ester moiety[1].

Synthesis

SINOVA SL-03967

107259-05-2

tert-Butyl (1-(hydroxymethyl)cyclopropyl)carbamate

107017-73-2

General procedure for the synthesis of (1-hydroxymethylcyclopropyl)-tert-butoxycarbonylamino acids from ethyl 1-(BOC-amino)cyclopropanecarboxylate: ethyl 1-((tert-butoxycarbonyl)amino)cyclopropanecarboxylate (4.31 g, 18.80 mmol) was dissolved in tetrahydrofuran (THF, 20 mL), and a 2M lithium borohydride (LiBH4) THF solution was slowly added dropwise ( 10.34 mL, 20.68 mmol), and the reaction mixture was stirred at room temperature overnight. Subsequently, a THF solution of 2M LiBH4 (5 mL, 10 mmol) was added additionally and stirring was continued at room temperature for 6 hours. Upon completion of the reaction, anhydrous sodium sulfate (Na2SO4, 15 g) and water (H2O, 10 mL) were added and the suspension was stirred at room temperature over the weekend. The suspension was filtered through a pad of sodium sulfate and the residue was washed with dichloromethane (DCM). The combined filtrates were concentrated under reduced pressure and the product was purified by column chromatography (silica gel, heptane/ethyl acetate, 1:1) to give 2.78 g of the target product in 79% yield.

References

[1] Brackmann F, et al. Synthesis of Spirocyclopropanated Analogues of Imidacloprid and Thiacloprid. European Journal of Organic Chemistry, 2005; 2005: 600-609.
[2] Brackmann F, et al. Synthesis of Spirocyclopropanated Analogues of Iprodione. European Journal of Organic Chemistry, 2005; 2005: 2250-2258.

24424-99-5
115652-52-3
107017-73-2
Synthesis of tert-Butyl (1-(hydroxymethyl)cyclopropyl)carbamate from Di-tert-butyl dicarbonate and 1-Amino-1-(hydroxymethyl)cyclopropane hydrochloride
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View Lastest Price from tert-Butyl (1-(hydroxymethyl)cyclopropyl)carbamate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
N-BOC-1-AMINO-CYCLOPROPANEMETHANOL  pictures 2025-11-18 N-BOC-1-AMINO-CYCLOPROPANEMETHANOL
107017-73-2
$1.10 1g 99.0% Min 100 Tons Dideu Industries Group Limited
Boc-1-Aminocyclopropylmethanol pictures 2025-04-04 Boc-1-Aminocyclopropylmethanol
107017-73-2
1kg 98% 1Ton Henan Aochuang Chemical Co.,Ltd.
N-BOC-1-AMINO-CYCLOPROPANEMETHANOL pictures 2019-09-05 N-BOC-1-AMINO-CYCLOPROPANEMETHANOL
107017-73-2
$5.50 2KG 96%-99% 100kg Career Henan Chemical Co

tert-Butyl (1-(hydroxymethyl)cyclopropyl)carbamate Spectrum

Boc-1-Aminocyclopropylmethanol 1-(Boc-amino)cyclopropylmethanol [1-(Hydroxymethyl)cyclopropyl]carbamicacid tert-butyl ester Carbamicacid, [1-(hydroxymethyl)cyclopropyl]-, 1,1-dimethylethyl ester (9CI) Boc-ACPC-ol tert-butyl 2-(1-aMinocyclopropyl)-2-hydroxyacetate (1-HydroxyMethyl-cyclopropyl)-carbaMic acid tert-b 2-Methyl-2-propanyl [1-(hydroxyMethyl)cyclopropyl]carbaMate [1-(tert-ButoxycarbonylaMino)cyclopropyl]Methanol N-Boc-1-AMinocyclopropylMethanol 1-(Boc-amino)cyclopropylmethanol N-Boc-1-amino-cyclopropanemethanol [1-(tert-Butoxycarbonylamino)cyclopropyl]methanol Boc-1-aminocyclopropane methanol TERT-BUTYL 1-(HYDROXYMETHYL)CYCLOPROPYLCARBAMATE(WX640242) [1-(tert-Butoxycarbonylamino)cyclopropyl]methanol > Carbamic acid, N-[1-(hydroxymethyl)cyclopropyl]-, 1,1-dimethylethyl ester N-BOC-1-AMINO-CYCLOPROPANEMETHANOL ISO 9001:2015 REACH SKL325 tert-Butyl [1-(Hydroxymethyl)cyclopropyl]carbamate 1-Boc-Amino-cyclopropanemethanol Boc-1-Amnocyclopropylmethanol N-BOC-1-AMINO-CYCLOPROPANEMETHANOL tert-butyl N-[1-(hydroxymethyl)cyclopropyl]carbamate 107017-73-2
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