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3232-26-6

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3232-26-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3232-26-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,3 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3232-26:
(6*3)+(5*2)+(4*3)+(3*2)+(2*2)+(1*6)=56
56 % 10 = 6
So 3232-26-6 is a valid CAS Registry Number.

3232-26-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-butyl-1,3,5-triazine-2,4-diamine

1.2 Other means of identification

Product number -
Other names 1,3,5-Triazine-2,4-diamine,6-butyl

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:3232-26-6 SDS

3232-26-6Downstream Products

3232-26-6Relevant articles and documents

2,4,6-trisubstituted-1,3,5-s-triazine compound and preparation and application thereof

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Paragraph 0028-0029; 0074-0075, (2021/10/05)

The invention provides a 2,4,6-trisubstituted-1,3,5-s-triazine compound as well as preparation and application thereof, and biguanide or dimethyl biguanide hydrochloride is used as an initial raw material to react with a cyano compound under an alkaline condition to prepare the 2,4,6-trisubstituted-1,3,5-s-triazine compound. The invention provides a simple and convenient synthetic method of a 2,4,6-trisubstituted-1,3,5-s-triazine compound, and the compound provided by the invention can be applied to preparation of an anti-myelogenous leukemia medicine, namely an enasidenib medicine. Compared with the prior art, the method for preparing the enasidenib has the advantages that two-step reaction is reduced, the use of a halogenating reagent is avoided, and the method is a green and environment-friendly chemical process. The structural formula I is shown in the specification.

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