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138792-65-1

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138792-65-1 Usage

Bicyclic structure

Yes

Class of compounds

Benzodiazepine

Central nervous system effects

Depressant

Sedative properties

Yes

Hypnotic properties

Yes

Anxiolytic properties

Yes

Stereochemistry

1-alpha-, 3-alpha-, 5-alpha-

Classification

Dihydrobenzodiazepine

Pharmaceutical use

Yes

Therapeutic applications

Treatment of anxiety, insomnia, and other neurological disorders

Side effects

Range of side effects associated with benzodiazepines

Potential for dependence

Yes

Withdrawal symptoms

Potential for withdrawal symptoms upon discontinuation

Check Digit Verification of cas no

The CAS Registry Mumber 138792-65-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,7,9 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 138792-65:
(8*1)+(7*3)+(6*8)+(5*7)+(4*9)+(3*2)+(2*6)+(1*5)=171
171 % 10 = 1
So 138792-65-1 is a valid CAS Registry Number.

138792-65-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,5-Ethano-2H-1,5-benzodiazepin-3-ol,3,4-dihydro-,(1-α-,3-α-,5-α-)-(9CI)

1.2 Other means of identification

Product number -
Other names benzo<f>-1,5-diazabicyclo<3.2.2>nonen-1-ol

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:138792-65-1 SDS

138792-65-1Relevant articles and documents

DIAZABICYCLOALKANES WITH BRIDGING NITROGEN ATOMS. 23. SYNTHESIS AND PROPERTIES OF BENZO-1,5-DIAZABICYCLONONEN-3-OL

Doronina, S. O.,Gall', A. A.,Shishkin, G. V.,Mamatyuk, V. I.,Sal'nikov, G. E.

, p. 779 - 782 (2007/10/02)

Intramolecular cyclization 1-(2-hydrohyethyl)-2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-3-ol gives benzo-1,5-diazabicyclononen-3-ols.Further treatment with acetic anhydride gives their 3-acetyl derivatives.The stereoisomers have been separated and their substituent configurations shown by PMR spectroscopy.

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