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168648-78-0

168648-78-0

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168648-78-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 168648-78-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,8,6,4 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 168648-78:
(8*1)+(7*6)+(6*8)+(5*6)+(4*4)+(3*8)+(2*7)+(1*8)=190
190 % 10 = 0
So 168648-78-0 is a valid CAS Registry Number.

168648-78-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (6aS,11aS)-3-methoxy-5-(4-methylphenyl)sulfonyl-9-phenylmethoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]quinolin-8-ol

1.2 Other means of identification

Product number -
Other names Benzofuro(3,2-c)quinolin-8-ol,5,6,6a,11a-tetrahydro-3-methoxy-5-((4-methylphenyl)sulfonyl)-9-(phenylmethoxy)-,cis

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:168648-78-0 SDS

168648-78-0Downstream Products

168648-78-0Relevant articles and documents

Stereoselective syntheses of substituted pterocarpans with anti-HIV activity, and 5-aza-/5-thia-pterocarpan and 2-aryl-2,3-dihydrobenzofuran analogues

Engler, Thomas A.,LaTessa, Kenneth O.,Iyengar, Rajesh,Chai, Wenying,Agrios, Konstantinos

, p. 1755 - 1769 (2007/10/03)

Oxygenated pterocarpans and 5-azapterocarpans are prepared utilizing Lewis acid-promoted reactions of 2-alkoxy-1,4-benzoquinones with 2H-chromenes and N-tosyl-1,2-dihydroquinolines, respectively. Similarly, benzannulated analogues are prepared via reactions of 5-aIkoxy-1,4-naphthoquinones with chromenes, and related 2-aryl-2,3-dihydrobenzofurans result from reactions of styrenes with the quinones. Syntheses of 5-thiapterocarpans are also described utilizing Pd(0)-coupling of o-chloromercuriophenols with 2H-chromenes.

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