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Cyclohexanecarboxaldehyde, 4-methylene- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89402-20-0

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89402-20-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89402-20-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,4,0 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 89402-20:
(7*8)+(6*9)+(5*4)+(4*0)+(3*2)+(2*2)+(1*0)=140
140 % 10 = 0
So 89402-20-0 is a valid CAS Registry Number.

89402-20-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methylidenecyclohexane-1-carbaldehyde

1.2 Other means of identification

Product number -
Other names 4-Methylenecyclohexanecarboxaldehyde

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:89402-20-0 SDS

89402-20-0Downstream Products

89402-20-0Relevant academic research and scientific papers

Control of transient aluminum-aminals for masking and unmasking reactive carbonyl groups

Barrios, Francis J.,Springer, Brannon C.,Colby, David A.

supporting information, p. 3082 - 3085 (2013/07/26)

A new reagent, the dimethylaluminum N,O-dimethylhydroxylamine complex, is effective at masking reactive carbonyl groups in situ from nucleophilic addition. This reagent allows chemoselective addition of reducing reagents, Grignard reagents, organolithiums, Wittig reagents, and enolates into substrates with multiple carbonyl groups. Moreover, the trapped carbonyl group, a stable aminal, can be unmasked in situ for additional synthetic manipulations.

Alicyclic substituted oxazolidine-2,4-diones having hypoglycemic activity

-

, (2008/06/13)

Hypoglycemic oxazolidine-2,4-diones, substituted at the 5-position with a (C5 -C9) unsaturated monocyclic, saturated bicyclic or unsaturated bicyclic hydrocarbon radical; methods for their preparation; and method for their use in the

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