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8-nitro-4-phenyl-1,3-dihydro-2H-1,5-benzodiazepin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63614-65-3

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63614-65-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63614-65-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,6,1 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 63614-65:
(7*6)+(6*3)+(5*6)+(4*1)+(3*4)+(2*6)+(1*5)=123
123 % 10 = 3
So 63614-65-3 is a valid CAS Registry Number.

63614-65-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-nitro-4-phenyl-1,3-dihydro-2H-1,5-benzodiazepin-2-one

1.2 Other means of identification

Product number -
Other names 8-Nitro-4-phenyl-2,3-dihydro-1H-1,5-benzodiazepin-2-one

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:63614-65-3 SDS

63614-65-3Downstream Products

63614-65-3Relevant academic research and scientific papers

Synthesis of 1H-1,5-benzodiazepin-2(3H)-ones from 5(4H)-isoxazolone, a heterocyclic bifunctional C-3 synthon

Rao,Reddy,Veeranagaiah

, p. 446 - 448 (2007/10/02)

Unsubstituted and 7- or 8-substituted 4-aryl-1H-1,5-benzodiazepin-2(3H)-ones 3a-t have been synthesized by the condensation of 3-aryl-5(4H)-isoxazolones 1a-e and parent 4-substituted 1,2-benzenediamines 2a-d under acidic conditions.

SYNTHESIS OF 1,5-BENZODIAZEPINES

Ushirogochi, Atsuyuki,Tominaga, Yoshinori,Matsuda, Yoshiro,Kobayashi, Goro

, p. 7 - 10 (2007/10/02)

Reaction of α-oxoketene S,S-acetals (1a, b, c, d) with o-phenylenediamines gave the corresponding 1,5-benzodiazepines, 8-substituted 4-aryl-2-methylthio-3H-1,5-benzodiazepines (3a, b, c, d, e) in good yields. 2-Amino-4-aryl-8-nitro-3H-1,5-benzodiazepines (5a, b, c) were prepared by the displacement of methylthio group on compound 3b with amines (benzylamine, morpholine, 1-methylpiperazine).

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