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Methanone, (2-hydroxy-4,6-dimethoxyphenyl)(2-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61736-75-2

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61736-75-2 Usage

Preparation

Obtained by partial demethylation of 2,4,6-trimethoxy-2′-nitrobenzophenone with boron tribromide in methylene chloride at 0° for 10 min and at r.t. overnight (97%).

Check Digit Verification of cas no

The CAS Registry Mumber 61736-75-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,7,3 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 61736-75:
(7*6)+(6*1)+(5*7)+(4*3)+(3*6)+(2*7)+(1*5)=132
132 % 10 = 2
So 61736-75-2 is a valid CAS Registry Number.

61736-75-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-hydroxy-4,6-dimethoxyphenyl)-(2-nitrophenyl)methanone

1.2 Other means of identification

Product number -
Other names 4,6-dimethoxy-2-hydroxy-2'-nitrobenzophenone

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:61736-75-2 SDS

61736-75-2Relevant academic research and scientific papers

RUTACEOUS CONSTITUENTS-13 A BIOMIMETIC SYNTHESIS OF ACRONYCINE

Adams, Joyce H.,Brown, P. Margaret,Gupta, Padma,Khan, M. Shafig,Lewis, John R.

, p. 209 - 218 (2007/10/02)

A biomimetic synthesis of the anti-tumor active alkaloid acronycine (7; R=R'=Me) has been obtained by cyclisation of 6-(2-methylaminobenzoyl)-5,7-dimethoxy-2,2-dimethylchromene (11; R=R'=Me); isoacronycine (20; R=R'=Me) was also produced.In an analogous manner the aminochromene (11; R=H, R'=Me) gave a mixture of des-N-methylacronycine (7; R=H, R'=Me) and des-N-methylisoacronycine (20; R=H, R'=Me).The aminochromenes were best synthesised by condensation of lithio-5,7-dimethoxy-2,2-dimethylchromene (22; R=Li) with N-methylisatoic anhydride (26) or with 2-methyl-3,1-benzoxazin-4-one (21).The relevance of this synthetic route to the biogenesis of acridone alkaloids is discussed.

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