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1215-52-7

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1215-52-7 Usage

Type of compound

Organic compound

Structure

Hydrazine derivative with a benzoyl group attached to one end and a benzyl group attached to the hydrazine nitrogen

Applications

a. Organic synthesis
b. Medicinal chemistry
c. Precursor for the synthesis of various heterocycles and organic compounds

Potential as an antineoplastic agent

Inhibits the growth of cancer cells

Other properties

a. Anticonvulsant
b. Antihypertensive

Significance

Versatile and potentially valuable compound in pharmaceutical research and development

Check Digit Verification of cas no

The CAS Registry Mumber 1215-52-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,1 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1215-52:
(6*1)+(5*2)+(4*1)+(3*5)+(2*5)+(1*2)=47
47 % 10 = 7
So 1215-52-7 is a valid CAS Registry Number.

1215-52-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-Benzylbenzohydrazide

1.2 Other means of identification

Product number -
Other names N'-benzylbenzoylhydrazide

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:1215-52-7 SDS

1215-52-7Relevant articles and documents

A convenient way for alkylation of amines using xanthate esters

Sukrutha, Kodipura P.,Swaroop, Toreshettahally R.,Preetham, Ramesh,Lokanath, Neratur K.,Rangappa, Kanchugarakoppal S.,Sadashiva, Maralinganadoddi P.

, p. 2316 - 2323 (2021/06/14)

N-alkylation of amines by the reaction with xanthate esters in the presence of acetic acid catalyst in ethanol is reported. Short reaction time, high yield, general applicability and environmentally benign nature are the noteworthy features of our protocol. The probable mechanism for the formation N-alkylation of amines is proposed.

One-Pot Synthesis of Protected Benzylhydrazines from Acetals

Mastitski, Anton,Niinepuu, Siret,Haljasorg, T?iv,J?rv, Jaak

, p. 416 - 423 (2018/10/25)

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Method for preparing secondary amine or N'-alkyl hydrazide through nickel catalysis N-alkylation reaction

-

Paragraph 0104; 0105; 0106; 0107; 0108, (2017/12/27)

The invention discloses a method for preparing secondary amine or N'-alkyl hydrazide through nickel catalysis N-alkylation reaction. Amine or hydrazide is used as raw materials; alcohol is used as an alkylation agent; N-alkylation reaction is performed under the nickel catalysis condition; the secondary amine or N'-alkyl hydrazide is prepared. Compared with the prior art, the method provided by the invention has the advantages that the N-alkylation reaction is performed; active catalysts can be generated in situ by nickel salt and phosphine ligands; the preparation of catalysts in advance is avoided; the operation is simple and convenient; the experiment steps and the experiment cost are reduced. Cheap nickel is used as the catalysts; the consumption of the catalysts is low; the use of expensive and high-toxicity precious metal is avoided; the experiment cost is further reduced; the hydrogen borrowing strategy is utilized; the N'-alkylation of the hydrazide is realized for the first time; byproducts only contain water. Compared with other preparation methods, the method has the advantage that the reaction environment-friendly performance is realized.

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