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3560-86-9

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3560-86-9 Usage

Chemical class

Guanidine derivatives

Usage

Catalyst in organic reactions

Specific application

Synthesis of polyurethane foams and elastomers

Structural feature

Unique structure enabling bifunctional catalysis

Role in polyurethane synthesis

Promotes urethane formation and blowing reactions

Reactivity

High

Selectivity

High

Industrial applications

Production of polyurethane materials

Additional studies

Potential antiviral and antibacterial properties

Potential applications

Pharmaceutical and medical fields

Check Digit Verification of cas no

The CAS Registry Mumber 3560-86-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,6 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3560-86:
(6*3)+(5*5)+(4*6)+(3*0)+(2*8)+(1*6)=89
89 % 10 = 9
So 3560-86-9 is a valid CAS Registry Number.

3560-86-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-bis(benzylideneamino)guanidine

1.2 Other means of identification

Product number -
Other names N,N'-bis-benzylidenamino-guanidine

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:3560-86-9 SDS

3560-86-9Relevant articles and documents

THE SYNTHESIS AND CYCLISATIOM OF THIOACYLATED DIAMINOGUANIDINES

Kurzer, Frederic,Secker, Jane L.

, p. 1429 - 1436 (2007/10/02)

The thiobenzoylation of 1,2-diaminoguanidine yields 1-amino-2-thioaroylamidoguanidines which are isolable as their stable hydrazones.They are unaffected by alkalis, but are cyclised by mineral acids, with loss of ammonia, to hydrazones of 2-aryl-5-hydrazino-1,3,4-thiadiazoles, or with elimination of hydrazine, to the appropriate 2-amino-5-aryl-1,3,4-thiadiazoles.The action of acetic anhydride effects the same ring-closures, yielding the corresponding acetylated products. 1,2-Diamino-3-phenylguanidine undergoes a comparable series of reactions.

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