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Phenol, 4-(bromomethyl)-, benzenesulfonate is a chemical compound with the molecular formula C13H13BrO4S. It is a derivative of phenol, where a bromine atom is attached to the methyl group, and a benzenesulfonate group is present. Phenol, 4-(bromomethyl)-, benzenesulfonate is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It is known for its reactivity and can undergo various chemical transformations, such as nucleophilic substitution and elimination reactions. Due to its potential applications in the synthesis of various products, Phenol, 4-(bromomethyl)-, benzenesulfonate is a valuable compound in the field of organic chemistry.

1836-70-0

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1836-70-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1836-70-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,3 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1836-70:
(6*1)+(5*8)+(4*3)+(3*6)+(2*7)+(1*0)=90
90 % 10 = 0
So 1836-70-0 is a valid CAS Registry Number.

1836-70-0SDS

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 benzenesulfonic acid 4-bromomethyl-phenyl ester

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 -
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More Details:1836-70-0 SDS

1836-70-0Upstream product

1836-70-0Relevant academic research and scientific papers

Synthetic studies toward spiroleucettadine

Chang, Jonah J.,Chan, Bryan,Ciufolini, Marco A.

, p. 3599 - 3601 (2007/10/03)

Synthetic hydroxydienone precursors to spiroleucettadine and to an isomer thereof resist cyclization to the orthoamide-type functionality present in the proposed structure of the natural product.

Environmentally-friendly Wohl-Ziegler bromination: Ionic-liquid reaction and solvent-free reaction

Togo, Hideo,Hirai, Takeshi

, p. 702 - 704 (2007/10/03)

Environmentally-friendly Wohl-Ziegler bromination of benzylic methyl groups was successfully camed out in ionic-liquid and solvent-free systems, to produce the corresponding benzylic bromides in good to moderate yields.

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