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61568-51-2

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61568-51-2 Usage

General Description

4-Bromobenzaldehyde propylidene acetal is a chemical compound with the molecular formula C11H11BrO2. It is a colorless to pale-yellow liquid that is primarily used as an intermediate in organic synthesis. 4-BROMOBENZALDEHYDE PROPYLIDENE ACETAL is commonly used in the manufacture of pharmaceuticals, agrochemicals, and other fine chemicals. It is also utilized as a reagent in various chemical reactions, including condensation and acetal formation. Additionally, 4-Bromobenzaldehyde propylidene acetal has applications in the flavor and fragrance industry, particularly in the synthesis of aroma chemicals. Overall, this compound is a versatile and important building block in the production of various chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 61568-51-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,6 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 61568-51:
(7*6)+(6*1)+(5*5)+(4*6)+(3*8)+(2*5)+(1*1)=132
132 % 10 = 2
So 61568-51-2 is a valid CAS Registry Number.

61568-51-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-BROMOBENZALDEHYDE PROPYLIDENE ACETAL

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:61568-51-2 SDS

61568-51-2Relevant articles and documents

"Post-it" type connected DNA created with a reversible covalent cross-link

Toms-Gamasa, Mara,Serdjukow, Sascha,Su, Meng,Müller, Markus,Carell, Thomas

, p. 796 - 800 (2015)

We report the development of a new heterobase that is held together through reversible bonding. The so-formed cross-link adds strong stabilization to the DNA duplex. Despite this, the cross-link opens and closes through reversible imine bonding. Moreover,

PD-1/PD-L1 INHIBITORS

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Page/Page column 521, (2018/11/22)

Compounds according to formula (I), methods of using said compounds singly or in combination with additional agents and compositions of said compounds for the treatment of cancer are disclosed.

A METHOD OF ACETALIZING AN ALDEHYDE

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Page/Page column 22; 23; 24, (2013/09/26)

A method of acetalizing an aldehyde comprising reacting said aldehyde with an alcohol in the presence of a polymeric catalyst to form an acetal wherein the polymeric catalyst is a mesoporous poly-melamine-formaldehyde polymer.

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