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3-CHLORO-4'-METHOXY-3'-NITROBENZOPHENONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66938-41-8

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66938-41-8 Usage

Chemical Properties

LIGHT YELLOW POWDER

Check Digit Verification of cas no

The CAS Registry Mumber 66938-41-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,9,3 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 66938-41:
(7*6)+(6*6)+(5*9)+(4*3)+(3*8)+(2*4)+(1*1)=168
168 % 10 = 8
So 66938-41-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H10ClNO4/c1-20-13-6-5-10(8-12(13)16(18)19)14(17)9-3-2-4-11(15)7-9/h2-8H,1H3

66938-41-8SDS

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 (3-chlorophenyl)-(4-methoxy-3-nitrophenyl)methanone

1.2 Other means of identification

Product number -
Other names 3-chlorophenyl 4-methoxy-3-nitrophenyl ketone

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:66938-41-8 SDS

66938-41-8Relevant academic research and scientific papers

Synthesis of LIAZAL, a retinoic acid metabolism blocking agent (RAMBA) with potential clinical applications in oncology and dermatology.

Freyne,Raeymaekers,Venet,Sanz,Wouters,De Coster,Wauwe

, p. 267 - 272 (2007/10/03)

The synthesis of LIAZAL (compound 9, R085246) is described. LIAZAL inhibits all-trans-retinoic acid metabolism and thereby exerts retinoid-like effects in vivo.

Synthesis and anthelminthic acitivity of alkyl-(5-acyl-1-benzimidazol-2-yl) carbamates

Raeymackers,Van Gelder,Roevens,Janssen

, p. 586 - 594 (2007/10/05)

A series of alkyl-(5-acyl-l-H-benzimidazol-2-yl)-carbamates were prepared and screened for anthelminthic activity. Some of them were found to be fully active at low, atoxic oral dose levels against gastro-intestinal nematodes. The activity against Syphacia muris and Strongyloides ratta is indicated. From these studies methyl (5-benzoyl-1-H-benzimidazol-2-yl) carbamate (mebendazole) and methyl [5-(4-fluorobenzoyl)-1-H-benzimidazol-2-yl]carbamate (flubendazole) were selected for detailed investigation.

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