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Carbonic acid methyl(p-bromophenyl) ester, also known as methyl 4-bromophenyl carbonate, is an organic compound with the chemical formula C8H7BrO3. It is a colorless to pale yellow liquid that is soluble in organic solvents. This ester is synthesized by the reaction of carbonic acid with methyl p-bromophenyl, and it is used as an intermediate in the production of various pharmaceuticals and agrochemicals. Due to its reactivity, it is important to handle Carbonic acid methyl(p-bromophenyl) ester with care, as it can be harmful if inhaled, ingested, or absorbed through the skin.

1847-93-4

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1847-93-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1847-93-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,4 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1847-93:
(6*1)+(5*8)+(4*4)+(3*7)+(2*9)+(1*3)=104
104 % 10 = 4
So 1847-93-4 is a valid CAS Registry Number.

1847-93-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Kohlensaeure-[4-brom-phenyl]-methyl-ester

1.2 Other means of identification

Product number -
Other names Kohlensaeure-(4-brom-phenyl)-methyl-ester

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:1847-93-4 SDS

1847-93-4Relevant academic research and scientific papers

Light-induced synthesis of unsymmetrical organic carbonates from alcohols, methanol and CO2under ambient conditions

Saini, Sandhya,Gour, Nand Kishor,Khan, Shafiur Rehman,Deka, Ramesh Chandra,Jain, Suman L.

supporting information, p. 12800 - 12803 (2021/12/13)

The present work describes the first visible light-assisted, metal-free and organic base 1,1,3,3-tetramethyl guanidine (TMG) mediated synthesis of unsymmetrical methyl aryl/alkyl carbonates from the reaction of alcohols, methanol, and CO2 in high to excel

Indium-catalyzed reaction for the synthesis of carbamates and carbonates: selective protection of amino groups

Kim, Joong-Gon,Jang, Doo Ok

experimental part, p. 2688 - 2692 (2009/08/09)

We developed a simple, efficient, and selective method for preparing organic carbamates and carbonates using a catalytic amount of indium. A wide range of carbamates and carbonates were synthesized in high yields. The method is also applicable to the selective protection of amino groups under mild conditions.

Pentaalkylguanidines as etherification and esterification catalysts

Barcelo, Gerard,Grenouillat, Denis,Senet, Jean-Pierre,Sennyey, Gerard

, p. 1839 - 1848 (2007/10/02)

Several pentaalkylguanidines have been prepared and found to be superior catalysts for the preparation of aryl and aralkyl ethers from carbonates and for the methylation of phenols with dimethylcarbonate.They also act as effective catalysts for esterification of acids with alkyl chloroformates but not for the acetylation of tertiary alcohols with acetic anhydride.

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