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644-26-8

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644-26-8 Usage

Safety Profile

intraperitoneal routes. When heated to decomposition it emits toxicfumes of NOx.

Check Digit Verification of cas no

The CAS Registry Mumber 644-26-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,4 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 644-26:
(5*6)+(4*4)+(3*4)+(2*2)+(1*6)=68
68 % 10 = 8
So 644-26-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H21NO2/c1-5-14(2,11-15(3)4)17-13(16)12-9-7-6-8-10-12/h6-10H,5,11H2,1-4H3

644-26-8SDS

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 [1-(dimethylamino)-2-methylbutan-2-yl] benzoate

1.2 Other means of identification

Product number -
Other names Amyleine

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:644-26-8 SDS

644-26-8Downstream Products

644-26-8Relevant articles and documents

Aminomethyltriorganotin compounds, preferably α-mono or disubstituted; and the method of preparation

-

, (2008/06/13)

The invention concerns a method of preparation of aminomethyltriorganotin compounds, preferably α-mono or disubstituted, the new tin compounds obtained thereby and an application of said tin compounds to the synthesis of aminomethylorganometallic compounds and to the regiospecific preparation of β-aminoalcohols. The intermediate tin and metallic compounds are new. The method for preparing the tin compounds comprises reacting an iminium salt with a corresponding stannylanion, preferably a triorganostannylanion. This method provides best yields and provides regiospecific β-aminoalcohols useful by having in most cases a large spectrum of pharmacological activities.

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