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73274-87-0

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73274-87-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73274-87-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,2,7 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 73274-87:
(7*7)+(6*3)+(5*2)+(4*7)+(3*4)+(2*8)+(1*7)=140
140 % 10 = 0
So 73274-87-0 is a valid CAS Registry Number.

73274-87-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dihydro-3-hydroxy-7-methoxyisobenzofuran-1-one

1.2 Other means of identification

Product number -
Other names 3-hydroxy-7-methoxy-1(3H)-isobenzofuranone

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:73274-87-0 SDS

73274-87-0Relevant articles and documents

Inhibitors of protein activity for the treatment of angiogenesis and SOX18/or lymphangiogenesis-related diseases

-

, (2020/01/04)

Disclosed are compounds of a formula provided herein that show efficacy in the inhibition of SOX18 protein activity, and in particular with respect to the ability of SOX18 to bind DNA and/or particular protein partners. Further, methods of treating angiog

Probing the reactivity of o-phthalaldehydic acid/methyl ester: Synthesis of N-isoindolinones and 3-arylaminophthalides

Mamidyala, Sreeman K.,Cooper, Matthew A.

, p. 8407 - 8409 (2013/09/23)

A new method for the synthesis of N-substituted isoindolinones and 3-arylaminophthalides was developed through aza-Wittig/cyclisation. The reaction of o-phthalaldehydic acid methyl ester with benzylic, aromatic and aliphatic azides gave N-isoindolinones w

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