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2-Butenoic acid, 2-methyl-, (5,8-dihydro-7-hydroxy-6-methyl-5,8-dioxo-1-isoquinolinyl)methyl ester, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77515-81-2

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77515-81-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77515-81-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,5,1 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 77515-81:
(7*7)+(6*7)+(5*5)+(4*1)+(3*5)+(2*8)+(1*1)=152
152 % 10 = 2
So 77515-81-2 is a valid CAS Registry Number.

77515-81-2SDS

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 (5,8-dihydro-7-hydroxy-6-methyl-5,8-dioxo-1-isoquinolinyl)methyl (2Z)-2-methyl-2-butenoate

1.2 Other means of identification

Product number -
Other names demethylrenierone

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:77515-81-2 SDS

77515-81-2Relevant academic research and scientific papers

Chemistry of renieramycins. Part 6: Transformation of renieramycin M into jorumycin and renieramycin J including oxidative degradation products, mimosamycin, renierone, and renierol acetate

Saito, Naoki,Tanaka, Chieko,Koizumi, Yu-Ichi,Suwanborirux, Khanit,Amnuoypol, Surattana,Pummangura, Sunibhond,Kubo, Akinori

, p. 3873 - 3881 (2007/10/03)

The transformation of renieramycin M (1m) into renieramycin J (1j) and jorumycin (2) is presented along with the results of antiproliferative assay data. The chemical stability and the oxidative degradation of 2 and renieramycin E (1e) to generate simple isoquinoline alkaloids, such as mimosamycin (7), renierol acetate (12), and renierone (8) are also described.

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