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807320-43-0

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807320-43-0 Usage

General Description

"Cis-1'-Oxo-spiro[cyclohexane-1,3'(1'H)-furo[3,4-c]pyridine]-4-carboxylic acid" is a chemical compound with a complex and unique structure. It contains a spiro ring system with a cyclohexane and furo[3,4-c]pyridine moiety, as well as a carboxylic acid functional group. The cis-1'Oxo configuration indicates the position of a ketone group on the spiro ring system. cis-1'-Oxo-spiro[cyclohexane-1,3'(1'H)-furo[3,4-c]pyridine]-4-carboxylic acid may have potential pharmaceutical or biological activities due to its intricate structure and functional groups. Its exact uses and properties would need to be further studied and determined through research and testing.

Check Digit Verification of cas no

The CAS Registry Mumber 807320-43-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,7,3,2 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 807320-43:
(8*8)+(7*0)+(6*7)+(5*3)+(4*2)+(3*0)+(2*4)+(1*3)=140
140 % 10 = 0
So 807320-43-0 is a valid CAS Registry Number.

807320-43-0SDS

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'-oxospiro[1,3'-cyclohexane(1'H)-furo[3,4-c]pyridine]-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names CIS-1'-OXO-SPIRO[CYCLOHEXANE-1,3'(1'H)-FURO[3,4-C]PYRIDINE]-4-CARBOXYLICACID

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:807320-43-0 SDS

807320-43-0Downstream Products

807320-43-0Relevant articles and documents

Practical synthesis of a neuropeptide Y antagonist via stereoselective addition to a ketene

Iida, Takehiko,Satoh, Hiroki,Maeda, Kenji,Yamamoto, Yuhei,Asakawa, Ken-Ichi,Sawada, Naotaka,Wada, Toshihiro,Kadowaki, Chie,Itoh, Takahiro,Mase, Toshiaki,Weissman, Steven A.,Tschaen, Dave,Krska, Shane,Volante

, p. 9222 - 9229 (2005)

The synthesis of neuropeptide Y antagonist 1, currently under clinical investigation for the treatment of obesity, is described. The convergent synthesis from trans-spirolactone carboxylic acid intermediate 2a and aminopyrazole 3 is predicated on a stereo

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