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76148-76-0

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76148-76-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76148-76-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,1,4 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 76148-76:
(7*7)+(6*6)+(5*1)+(4*4)+(3*8)+(2*7)+(1*6)=150
150 % 10 = 0
So 76148-76-0 is a valid CAS Registry Number.

76148-76-0SDS

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 2-amino-3-sulfanylnaphthalene-1,4-dione

1.2 Other means of identification

Product number -
Other names 2-mercapto-3-amino-1,4-naphthoquinone

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:76148-76-0 SDS

76148-76-0Relevant articles and documents

Sulfur-containing derivatives of 1,4-naphthoquinone, part 1: Disulfide synthesis

Stasevych, Maryna V.,Plotnikov, Maxym Yu.,Platonov, Mykola O.,Sabat, Svitlana I.,Musyanovych, Rostyslav Ya.,Novikov, Volodymyr P.

, p. 205 - 211 (2007/10/03)

Bisulfides of 1,4-naphthoquinone were synthesized, and different methods of their synthesis were investigated. High yields and purity of disulfides were obtained from the oxidation of thiol derivatives. The latter were prepared in high yields and purity from isothiuronic salts. The obtained disulfides are synthones for compounds with a wide spectrum of biological activity.

REACTION OF THIOAMIDES WITH 2,3-DICHLORO-1,4-NAPHTHOQUINONE. A NOVEL SYNTHESIS OF NAPHTHOTHIAZOLE-4,9-DIONES

Hammam, A.S.,Bayoumy, B.E.

, p. 71 - 79 (2007/10/02)

The reaction of thioamide II with 2,3-dichloro-1,4-naphthoquinone (I) in ethanol gave naphtho-thiazole-4,9-diones (IV).The intermediates, 2-thioamido-3-chloro-1,4-naphthoquinones III were also isolated from the reaction medium and could be separately transformed to IV by further boiling in aqueous ethanol containing bicarbonate.The reaction of thiosemicarbazide with I under similar conditions gave naphtho-2-amino-4H-1,3,4-thiadiazine-5,10-dione (VII).

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