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1H-1,5-Benzodiazepine, 2,3-dihydro-4-(4-methoxyphenyl)-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75220-81-4

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75220-81-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75220-81-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,2,2 and 0 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 75220-81:
(7*7)+(6*5)+(5*2)+(4*2)+(3*0)+(2*8)+(1*1)=114
114 % 10 = 4
So 75220-81-4 is a valid CAS Registry Number.

75220-81-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-methoxyphenyl)-2-phenyl-2,3-dihydro-1H-benzo[b][1,4]-diazepine

1.2 Other means of identification

Product number -
Other names -

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:75220-81-4 SDS

75220-81-4Relevant academic research and scientific papers

Synthesis and biological screening of some new 1,5-benzodiazepine derivatives as promising antibacterial and antitubercular agents

Monga, Vikramdeep,Nayak, Surendra Kumar,Singh, Gurpreet

, p. 143 - 149 (2020/07/21)

In this study, various substituted 1,5-benzodiazepines were synthesized by condensing different substituted chalcones with o-phenylenediamine in methanol using piperidine as a base under refluxing conditions and were obtained in good yield after purificat

Construction of the 1,5-Benzodiazepine Skeleton from o-Phenylendiamine and Propargylic Alcohols via a Domino Gold-Catalyzed Hydroamination/Cyclization Process

Cacchi, Sandro,Fabrizi, Giancarlo,Goggiamani, Antonella,Iazzetti, Antonia

supporting information, p. 3511 - 3513 (2016/08/16)

The gold-catalyzed reaction of o-phenylendiamine with propargylic alcohols affords 1,5-benzodiazepines bearing different substituents on the 2 and 4 positions. The method allows even for the selective preparation of 4-substituted 1,5-benzodiazepine derivatives.

Protic acidic ionic liquids promoted formation of 1,5-benzodiazepines: Remarkable effects of cations and anions on their performances

Du, Yuying,Tian, Fuli

, p. 486 - 489 (2007/10/03)

A series of protic acidic ionic liquids have been used as solvents and catalysts for the synthesis of 1,5-benzodiazepines. Success of the condensation appears to lie in the choice of cation-anion combinations and the ionic liquid [HBIm]CF3SOsu

Solvent-free synthesis of 1,5-benzothiazepines and benzodiazepines on inorganic supports

Kodomari, Mitsuo,Noguchi, Tomohiro,Aoyama, Tadashi

, p. 1783 - 1790 (2007/10/03)

1,5-Benzothiazepines and 1,5-benzodiazepines have been synthesized in solvent-free conditions from chalcones and o-aminothiophenol or o-phenylenediamine in the presence of inorganic support. Silica gel was found to be an effective support for the synthesi

On the mechanism and stereochemistry of the formation of β-lactam derivatives of 2,4-disubstituted-2,3-dihydro-benzo[1,4]diazepines

Wang,Zhou,Xu,Jin,Li,Chan

, p. 1031 - 1034 (2007/10/03)

2-Chloro-4-phenyl-2a-(4′-methoxyphenyl)-3,5-dihydroazatetracylic [1,2-d]benzo[1,4]diazepin-1-one (IIIa) and 2-chloro-4-phenyl-2a-(4′-methoxyphenyl)-3,5-dihydroazatetracyclic [1,2-d]benzo[1,4]diazepin-1-one(IIIb) were synthesized. 1-B

NEW ASPECTS OF THE CHEMISTRY OF 2,3-DIHYDRO-1H-1,5-BENZODIAZEPINE

Orlov, V. D.,Kolos, N. N.,Yaremenko, F. G.,Lavrushin, V. F.

, p. 547 - 550 (2007/10/02)

Under basic catalysis conditions the reaction of 4- and 4'-substituted chalcones with o-phenylenediamine leads to 2,3-dihydro-2,4-diaryl-1H-1,5-benzodiazepines; β-amino adducts, the ability of which to undergo intramolecular condensation increases as the

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