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54532-12-6

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54532-12-6 Usage

Chemical class

Derivative of hydrazine

Molecular structure

Complex, composed of a cyclohexylidene group and a dinitrophenyl group attached to the hydrazine molecule

Potential uses

Likely to have uses in chemistry and chemical research

Specific properties and applications

Not readily available

Reactivity

Presence of the tert-butyl and dinitrophenyl groups suggest that the compound may be reactive

Interest for further investigation

Potential reactivity with other chemicals makes it of interest for further investigation in the field of organic chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 54532-12-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,5,3 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 54532-12:
(7*5)+(6*4)+(5*5)+(4*3)+(3*2)+(2*1)+(1*2)=106
106 % 10 = 6
So 54532-12-6 is a valid CAS Registry Number.

54532-12-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(4-tert-butylcyclohexylidene)amino]-2,4-dinitroaniline

1.2 Other means of identification

Product number -
Other names t-Butyl-4-cyclohexanon-2,4-dinitrophenylhydrazon

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:54532-12-6 SDS

54532-12-6Relevant articles and documents

New applications of 1,5-hydrogen atom transfer reactions: Self-oxidizing protecting groups

Curran,Yu

, p. 123 - 127 (2007/10/02)

Three new alcohol protecting groups are introduced: o-bromobenzyl, o-bromo(methylenedioxy)benzyl, and o-bromotrityl. Removal of these protecting groups under reductive conditions with tributyltin hydride is coupled with an oxidation of the substrate to produce directly an aldehyde or ketone. This oxidation occurs by 1,5-hydrogen transfer, followed by β-fragmentation. For example, treatment of the o-bromobenzyl ether of 3-phenyl-1-propanol with tibutyltin hydride at 0.001 M (80°C) directly produces 3-phenyl-1-propanal. An application to the selective oxidation of primary alcohols in the presence of secondary alcohols is also introduced.

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