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(6-methoxy-1-oxo-tetralin-2-ylidene)methyl benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29113-13-1

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29113-13-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29113-13-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,1,1 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 29113-13:
(7*2)+(6*9)+(5*1)+(4*1)+(3*3)+(2*1)+(1*3)=91
91 % 10 = 1
So 29113-13-1 is a valid CAS Registry Number.

29113-13-1SDS

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-benzoyloxymethylene-6-methoxy-1-Tetralone

1.2 Other means of identification

Product number -
Other names 6-Methoxy-2-benzoyloxymethylen-1-tetralon

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:29113-13-1 SDS

29113-13-1Relevant academic research and scientific papers

FARNESYLATED TETRAHYDRO-NAPHTHALENOLS AS HYPOLIPIDEMIC AGENTS

-

, (2008/06/13)

The invention relates to novel farnesylated tetrahydro-naphthalenols, that inhibit HMGR activity which results in a decrease in serum total cholesterol, a decrease in LDL cholesterol levels, and inhibition of LDL oxidation. The farnesylated tetrahydro-nap

Synthesis and Stereochemical Studies on the Reductions of Some Pyrrole Derivatives

Bhattacharya, Sudin,Mandal, Asok N.,Chaudhuri, Swadesh R. Ray,Chatterjee, Amareshwar

, p. 5 - 13 (2007/10/02)

Total synthesis of the unique pyrrole derivatives (2a-d) and the steroid analogue (1) are reported.Reductions of the above imines with sodium borohydride or by a catalytic procedure have been found to be stereospecific, yielding only the trans-amine in ea

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