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3-Dehydroxy-3-oxo-4,5-dihydro OxazepaM is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19554-95-1

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19554-95-1 Usage

Uses

A degradation product of Oxazepam (O845700). Controlled Substance.

Check Digit Verification of cas no

The CAS Registry Mumber 19554-95-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,5,5 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19554-95:
(7*1)+(6*9)+(5*5)+(4*5)+(3*4)+(2*9)+(1*5)=141
141 % 10 = 1
So 19554-95-1 is a valid CAS Registry Number.

19554-95-1 Well-known Company Product Price

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  • USP

  • (1483017)  Oxazepam Related Compound A  United States Pharmacopeia (USP) Reference Standard

  • 19554-95-1

  • 1483017-15MG

  • 14,500.98CNY

  • Detail

19554-95-1SDS

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 7-chloro-5-phenyl-4,5-dihydro-1H-1,4-benzodiazepine-2,3-dione

1.2 Other means of identification

Product number -
Other names 7-Chlor-2,3-dioxo-5-phenyl-2,3,4,5-tetrahydro-1H-1,4-benzodiazepin

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:19554-95-1 SDS

19554-95-1Upstream product

19554-95-1Downstream Products

19554-95-1Relevant academic research and scientific papers

A one-step synthesis of [3-2H]Oxazepam

Yang,Bao,Shou

, p. 861 - 869 (1995)

The proton at 3-position, of oxazepam (7-chloro-1,3-dihydro-3-hydroxy-5-phenyl-2H-1,4-benzodiazepin-2-one) undergoes a deuterium exchange in deuterated alkaline methanol. A base-catalyzed keto-enol tautomerism is proposed to be responsible for the observe

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