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176236-88-7

176236-88-7

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176236-88-7 Usage

Chemical Properties

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Check Digit Verification of cas no

The CAS Registry Mumber 176236-88-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,2,3 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 176236-88:
(8*1)+(7*7)+(6*6)+(5*2)+(4*3)+(3*6)+(2*8)+(1*8)=157
157 % 10 = 7
So 176236-88-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H12O/c1-2-4-10-6-12-8-14-13(15-14)7-11(12)5-9(10)3-1/h1-6,13-14H,7-8H2/t13-,14+

176236-88-7SDS

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 2,3-EPOXY-1,2,3,4-TETRAHYDROANTHRACENE, 98

1.2 Other means of identification

Product number -
Other names 1a,2,9,9a-tetrahydroanthra[2,3-b]oxirene

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:176236-88-7 SDS

176236-88-7Relevant articles and documents

A general synthetic method for 2-substituted anthracenes

Dehaen, Wim,Corens, David,L'Abbe, Gerrit

, p. 201 - 203 (1996)

Anthracenes bearing a primary alkyl, ω-hydroxyalkyl, aryl or vinyl substituent at the 2-position are conveniently prepared by a copper-catalyzed Grignard reaction on 2,3-epoxy-1,2,3,4-tetrahydroanthracene, followed by dehydration - dehydrogenation of the resulting alcohols with tetrachloro-1,2-benzoquinone (o-chloranil).

Naphtho and benzo analogues of the κ opioid agonist trans-(±)-3,4-dichloro-N-methyl-N-[2-(1-pyrrolidinyl)cyclohexyl] benzeneacetamide

Freeman,Michalson,D'Andrea,Baczynskyj,VonVoigtlander,Lahti,Smith,Lawson,Scahill,Mizsak,Szmuszkovicz

, p. 1891 - 1896 (2007/10/02)

Further elaboration on the structure-activity relationships in our U-50,488 series has revealed that benzologation of this cyclohexane-1,2-diamine derivative provides compounds which either maintain the interaction with the κ receptor (e.g. compounds 3a a

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