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7651-40-3

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7651-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7651-40-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,5 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7651-40:
(6*7)+(5*6)+(4*5)+(3*1)+(2*4)+(1*0)=103
103 % 10 = 3
So 7651-40-3 is a valid CAS Registry Number.

7651-40-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-hex-3-yn-2-yl-5-prop-2-enyl-2-sulfanylidene-1,3-diazinane-4,6-dione

1.2 Other means of identification

Product number -
Other names RAC THIOHEXITAL

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:7651-40-3 SDS

7651-40-3Upstream product

7651-40-3Downstream Products

7651-40-3Relevant articles and documents

Chiral barbituric acid compound and preparation method thereof

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Paragraph 0024; 0027; 0030-0031, (2021/02/06)

The invention discloses a chiral barbituric acid compound and a preparation method thereof. The chiral barbituric acid compound is an optically active compound having a structure represented by the following formula (1), and comprises a levorotatory body or a dextrorotatory body having the same chemical general formula: in the formula: * represents a chiral carbon atom, substituent groups R1 and R3 are respectively and independently selected from alkyl, the substituent R2 is selected from alkyl or allyl, and X is selected from O or S. Racemic propargyl carbonate and malonate compounds are usedas initial raw materials, bis-(1, 5-cyclooctadiene) nickel metal is used as a catalyst, a chiral phosphine reagent is used as a ligand, Lewis acid is used as a co-catalyst, and asymmetric propargyl reaction and subsequent reduction and condensation reaction are performed under the assistance of alkali, the chiral barbituric acid compound is prepared with high yield, high enantioselectivity and approximate gram scale in an accurate and rapid mode for the first time, and the method has biomedical practicability and industrial application prospects.

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