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6373-60-0

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6373-60-0 Usage

Physical state

Yellow crystalline solid

Uses

a. Production of dyes and pigments
b. Intermediate in the synthesis of pharmaceuticals and other organic compounds

Toxicity

Moderate toxicity
a. Harmful effects on the respiratory system
b. Harmful effects on the skin

Environmental hazard

Potential environmental hazard

Handling and disposal

Should be handled and disposed of with care

Check Digit Verification of cas no

The CAS Registry Mumber 6373-60-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,7 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6373-60:
(6*6)+(5*3)+(4*7)+(3*3)+(2*6)+(1*0)=100
100 % 10 = 0
So 6373-60-0 is a valid CAS Registry Number.

6373-60-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-naphthoquinone-2-oxime

1.2 Other means of identification

Product number -
Other names [1,2]Naphthochinon-2-oxim

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:6373-60-0 SDS

6373-60-0Relevant articles and documents

EQUILIBRIA IN COMPLEXES OF N-HETEROCYCLIC MOLECULES. PART 30. REACTION OF 5-NITRO-1,10-PHENANTHROLINE WITH AQUEOUS BASES

Gillard, R. D.,Houghton, Roy P.,Tucker, John N.

, p. 2102 - 2107 (1980)

In water and in dimethyl sulphoxide, hydroxide anion adds reversibly to position 6 of 5-nitro-1,10-phenanthroline to give an anion whose equilibrium constant of formation (in water) at 20 deg C is 1.2 +/- 0.1 dm3 mol -1.When heated in aqueous media, this anion rearranges to the anion of the mono-oxime of 1,10-phenanthroline-5,6-quinone.A further reaction then affords ammonia in high yield and whose nitrogen atom is derived entirely from the nitro-group of the nitrophenanthroline, and 4,5-diazafluoren-9-one as the major organic product.

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