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138875-15-7

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138875-15-7 Usage

Chemical class

Benzodiazepine compound

Uses

Sedative, anxiolytic, and hypnotic medication

Mechanism of action

Modulates the activity of certain neurotransmitters in the brain, leading to a calming and relaxing effect

Commonly prescribed for

Treatment of anxiety, insomnia, and muscle spasms

Precautions

Should be used under the guidance of a healthcare professional

Potential for habit-forming

Yes

Side effects

Drowsiness, dizziness, and impaired coordination

Interactions with other medications and substances

May interact, so caution should be exercised when using it
Please note that this information is based on the material provided and is not a comprehensive list of all properties and content related to this chemical. It is always recommended to consult a healthcare professional for accurate and up-to-date information on medications and their uses.

Check Digit Verification of cas no

The CAS Registry Mumber 138875-15-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,8,7 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 138875-15:
(8*1)+(7*3)+(6*8)+(5*8)+(4*7)+(3*5)+(2*1)+(1*5)=167
167 % 10 = 7
So 138875-15-7 is a valid CAS Registry Number.

138875-15-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,8-DIAZATRICYCLO[6.3.2.02,7]TRIDECA-2,4,6-TRIEN-10-OL

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:138875-15-7 SDS

138875-15-7Relevant 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 (1991)

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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