Welcome to LookChem.com Sign In|Join Free
  • or
Carbonic acid, butyl (phenylthio)methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

185145-46-4

Post Buying Request

185145-46-4 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

185145-46-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 185145-46-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,1,4 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 185145-46:
(8*1)+(7*8)+(6*5)+(5*1)+(4*4)+(3*5)+(2*4)+(1*6)=144
144 % 10 = 4
So 185145-46-4 is a valid CAS Registry Number.

185145-46-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name butyl ((phenylthio)methyl) carbonate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:185145-46-4 SDS

185145-46-4Relevant academic research and scientific papers

Tin-Pummerer rearrangement in the synthesis of O,S-acetal derivatives

Hatlelid, Jostein,Benneche, Tore,Undheim, Kjell

, p. 1092 - 1095 (2007/10/03)

α-Thioalkyl esters and carbonates have been prepared by a tin-Pummerer rearrangement in reactions of α-stannylated sulfoxides with acid chlorides or chloroformates, respectively. Acid chlorides have a higher reactivity than chloroformates in this reaction. Acta Chemica Scandinavica 1997.

Cleavage of carbon-sulfur bonds in the synthesis of α-haloalkyl carbonates

Hatlelid, Jostein,Benneche, Tore,Undheim, Kjell

, p. 1041 - 1044 (2007/10/03)

α-Chloroalkyl and α-bromoalkyl carbonates have been prepared by cleavage of α-arylthioalkyl carbonates with sulfuryl chloride or bromine, respectively. The α-arylthioalkyl carbonates are prepared by reaction of the hemithioacetal 1 with chloroformates or by a destannylative tin-Pummerer rearrangement of α-stannyl sulfoxides. Acta Chemica Scandinavica 1996.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 185145-46-4