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76274-21-0

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76274-21-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76274-21-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,2,7 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 76274-21:
(7*7)+(6*6)+(5*2)+(4*7)+(3*4)+(2*2)+(1*1)=140
140 % 10 = 0
So 76274-21-0 is a valid CAS Registry Number.

76274-21-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-1-oxo-1,2-dihydronaphthalen-2-yl acetate

1.2 Other means of identification

Product number -
Other names -

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:76274-21-0 SDS

76274-21-0Relevant articles and documents

Oxidation of 1-Naphthols by Lead Tetraacetate in Acetic Acid

Greenland, Harry,Pinhey, John T.,Sternhell, Sever

, p. 2067 - 2074 (2007/10/02)

A detailed study of the lead tetraacetate-acetic acid oxidation of 1-naphthol, 4-acetoxy-1-naphthol, 2-methyl-1-naphthol, 2,3-dimethyl-1-naphthol and 1,2,3,4-tetrahydro-9-anthrol (17) has been carried out.In the case of 1-naphthol the major product was 4-acetoxy-1-naphthol (4), with 2,2-diacetoxynaphthalen-1(2H)-one (2) being the only other product formed in significant yield.Attack at C4 was again the main reaction with 4-acetoxy-1-naphthol, which gave 1,4-naphthoquinone as the major product.Acetoxylation occurred predominantly at C2 with 2-methyl-1-naphthol and 2,3-dimethyl-1-naphthol to give the naphthalen-1(2H)-ones (11) and (12) respectively.In both cases minor amounts of 4-acetoxylated derivatives and quinones were also produced. 1,2,3,4-Tetrahydro-9-anthrol (17) gave an analogous set of products, the yields of which showed as unusual concentration dependence.In dilute solution 10-acetoxy-1,2,3,4-tetrahydro-9-anthrol (19) was produced in high yield, whereas with a high substrate concentration a good yield of 9a-acetoxy-1,2,3,4-tetrahydroanthracen-9(9aH)-one (18) was obtained.

Oxidation of Halophenols and Highly Substituted Phenols with Lead(IV) Acetate

Perumal, P. Thirumalai,Bhatt, M. Vivekananda

, p. 943 - 945 (2007/10/02)

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