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104311-39-9

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104311-39-9 Usage

General Description

3,5-Diacetoxybenzylbromide is a chemical compound with the molecular formula C11H11BrO4. It is a derivative of benzylbromide, with acetoxy groups attached at the 3 and 5 positions of the benzene ring. 3,5-Diacetoxybenzylbromide is commonly used in organic synthesis as a reagent for the introduction of the benzyl group into various organic molecules. It is known for its ability to undergo nucleophilic substitution reactions, where the bromine atom is replaced by a nucleophile such as an alcohol or amine. 3,5-Diacetoxybenzylbromide is a versatile compound that finds application in the synthesis of various pharmaceuticals and fine chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 104311-39-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,3,1 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 104311-39:
(8*1)+(7*0)+(6*4)+(5*3)+(4*1)+(3*1)+(2*3)+(1*9)=69
69 % 10 = 9
So 104311-39-9 is a valid CAS Registry Number.

104311-39-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name acetic acid,5-(bromomethyl)benzene-1,3-diol

1.2 Other means of identification

Product number -
Other names 3,5-diacetoxybenzyl bromide

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:104311-39-9 SDS

104311-39-9Relevant articles and documents

Verification of the necessity of the tolyl group of PF-543 for sphingosine kinase 1 inhibitory activity

Baek, Dong Jae,Ki, Sung Hwan,Kim, Sang-Bum,Kim, Sanghee,Kim, Su Bin,Kwon, Yongseok,Lee, Joo-Youn,Lee, Taeho,Moon, Hong Seop,Oh, Yoon Sin,Park, Eun-Young,Park, Jeong-Eun

, (2020)

PF-543, the most potent sphingosine kinase (SK) inhibitor, does not demonstrate effective anticancer activity in some cancer cells, unlike other known SK1 inhibitors. PF-543 has a non-lipid structure with a unique toluene backbone; however, the importance

SYNTHESE DE CETONES SPIRANNIQUES TRICYCLIQUES DERIVEES DE PRODUITS NATURELS

Berrier, Christian,Jacquesy, Jean-Claude,Renoux, Alain

, p. 212 - 218 (2007/10/02)

In SbF5-HF compound 10a is unreactive whereas esters 10b and 10c cyclize to enones 18 (b or c) and 19 (b or c).Protonation of the esters groups prevents the corresponding aromatic ring protonation and deactivation which is observed with phenol 10a.Spiroke

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