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ChemicalBook >> CAS DataBase List >>Trichloromethanesulfonyl chloride

Trichloromethanesulfonyl chloride

CAS No.
2547-61-7
Chemical Name:
Trichloromethanesulfonyl chloride
Synonyms
Trichloromesyl chloride.;Trichlor-methansulfonylchlorid;trichloro-methanesulfonylchlorid;TRICHLOROMETHANESULFONYL CHLORIDE;trichloromethanesulphonyl chloride;Methanesulfonyl chloride, trichloro-;Trichloromethanesulfonyl Chloride >Trichloromethanesulfonyl chloride,pract.;TRICHLOROMETHANESULFONYL CHLORIDE, TECH.;trichloromethanesulfonyl chloride CCl4O2S
CBNumber:
CB2495941
Molecular Formula:
CCl4O2S
Molecular Weight:
217.89
MDL Number:
MFCD00007452
MOL File:
2547-61-7.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 00:45:49
Product description Number Pack Size Price
Trichloromethanesulfonyl chloride 97% 235962 5g $120
Trichloromethanesulfonyl Chloride >95.0%(T) T0611 5g $82
Trichloromethanesulfonyl Chloride >95.0%(T) T0611 25g $262
Trichloromethanesulfonyl chloride >95% OR72500 250mg $21
Trichloromethanesulfonyl chloride >95% OR72500 1g $33

Trichloromethanesulfonyl chloride Properties

Melting point 137-140 °C(lit.)
Boiling point 170°C
Density 1.8252 (estimate)
solubility soluble in Toluene
form solid
color White to Almost white
InChI 1S/CCl4O2S/c2-1(3,4)8(5,6)7
InChIKey ZCPSWAFANXCCOT-UHFFFAOYSA-N
SMILES ClC(Cl)(Cl)S(Cl)(=O)=O
CAS DataBase Reference 2547-61-7(CAS DataBase Reference)
NIST Chemistry Reference Methanesulfonyl chloride, trichloro-(2547-61-7)
EPA Substance Registry System Methanesulfonyl chloride, trichloro- (2547-61-7)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Corrosion (GHS05)Exclamation Mark (GHS07)
GHS05,GHS07
Signal word  Danger
Hazard statements  H314-H335
Precautionary statements  P260-P271-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338
target organs Respiratory system
PPE Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Hazard Codes  C
Risk Statements  34-36/37
Safety Statements  26-27-28-36/37/39-45
RIDADR  UN 3261 8/PG 2
WGK Germany  3
TSCA  TSCA listed
HS Code  2904.10.5000
HazardClass  8
PackingGroup  III
Storage Class 8A - Combustible corrosive hazardous materials
Hazard Classifications Eye Dam. 1
Skin Corr. 1B
STOT SE 3

Trichloromethanesulfonyl chloride price More Price(22)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 235962 Trichloromethanesulfonyl chloride 97% 2547-61-7 5g $120 2023-01-07 Buy
TCI Chemical T0611 Trichloromethanesulfonyl Chloride >95.0%(T) 2547-61-7 5g $82 2026-04-30 Buy
TCI Chemical T0611 Trichloromethanesulfonyl Chloride >95.0%(T) 2547-61-7 25g $262 2026-04-30 Buy
Apolloscientific OR72500 Trichloromethanesulfonyl chloride >95% 2547-61-7 250mg $21 2026-06-04 Buy
Apolloscientific OR72500 Trichloromethanesulfonyl chloride >95% 2547-61-7 1g $33 2026-06-04 Buy
Product number Packaging Price Buy
235962 5g $120 Buy
T0611 5g $82 Buy
T0611 25g $262 Buy
OR72500 250mg $21 Buy
OR72500 1g $33 Buy

Trichloromethanesulfonyl chloride Chemical Properties,Uses,Production

Application

Trichloromethanesulfonyl chloride can be used as a pharmaceutical synthesis intermediate. Perfluoroiodoalkanes and bromoalkanes undergo sulfinization-deiodination and debromination reactions with sodium dithionite under appropriate conditions, while perfluorochloroalkanes do not react under similar conditions. However, carbon tetrachloride and 1,1,1-trichloropolyfluoroalkanes can undergo sulfinization-dechlorination reactions with sodium dithionite. Trichlorobromomethane and trichloroiodomethane react under similar conditions to yield sulfinized debromination and deiodination products, respectively.

Uses

Trichloromethanesulfonyl chloride is an efficient free radical chlorinating agent. It reacts with pent-4-enylcobaloximes in inert solvent under tugsten lamp irradiation to yield 2-(β,β,β- trichloroethyl)sulfolanes. It also reacts with trimethylsilyl enol ethers of acetophenones in the presence of a ruthenium (II) phosphine complex to yield 1-aryl-3,3-dichloropropen-1-one and α-chloroacetophenones.

General Description

Trichloromethanesulfonyl chloride is an efficient free radical chlorinating agent. It reacts with pent-4-enylcobaloximes in inert solvent under tugsten lamp irradiation to yield 2-(β,β,β- trichloroethyl)sulfolanes. It also reacts with trimethylsilyl enol ethers of acetophenones in the presence of a ruthenium (II) phosphine complex to yield 1-aryl-3,3-dichloropropen-1-one and α-chloroacetophenones.

Synthesis

Step 1); reaction at 25C, under nitrogen atmosphere, 4.0g (26mmol) la, 4.6g (26mmol) sodium thiosulfate, 2.2g sodium bicarbonate, 18mL of water and 6mL of ethyl ether, stirred at 25C for 6h and then replenished with 2.3g of sodium thiosulfate, 1.1g of sodium bicarbonate, and continued to react for l0h, evaporated the solvent under reduced pressure, and extracted the leftover residual with 50mL of ethyl acetate. The solid was extracted three times with 50 mL of ethyl acetate, and the extract was de-esterified to give a white fluffy solid, which was crystallized by isopropanol to give 3.9 g of colorless crystals 2a in 73% yield. Step 2): 3.9g2a was dissolved in 15mL water, reacted with chlorine at 0 for lh, precipitated white solid, filtered, washed, dried, purified by sublimation method, obtained 3.9g of white solid trichloromethylsulfonyl chloride, yield 94%.

Trichloromethanesulfonyl chloride Preparation Products And Raw materials

Raw materials

Preparation Products

Trichloromethanesulfonyl chloride Suppliers

Global( 73)Suppliers
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TRICHLOROMETHANESULFONYL CHLORIDE Trichlor-methansulfonylchlorid trichloro-methanesulfonylchlorid Trichloromesyl chloride. TRICHLOROMETHANESULFONYL CHLORIDE, TECH. trichloromethanesulphonyl chloride Trichloromethanesulfonyl chloride,pract. trichloromethanesulfonyl chloride CCl4O2S Trichloromethanesulfonyl Chloride > Methanesulfonyl chloride, trichloro- 2547-61-7 Cl3CSO2Cl CCl4O2S Chlorination Halogenation Building Blocks Organic Building Blocks Sulfonyl Halides Sulfur Compounds Chlorination Halogenation Synthetic Organic Chemistry Organic Building Blocks Sulfonyl Halides Sulfur Compounds Building Blocks Chemical Synthesis Organic Building Blocks Sulfonyl Halides Sulfur Compounds
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