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1097-35-4

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1097-35-4 Usage

General Description

4-(Benzyloxy)-N-benzamidoaniline is a chemical compound with the molecular formula C22H19N3O2. It is a type of aniline derivative that contains a benzamide functional group and a benzyloxy group. 4-(BENZYLOXY)-N-BENZAMIDOANILINE is commonly used in organic synthesis and pharmaceutical research. It is known for its potential applications in the development of new drugs and pharmaceutical products, particularly in the field of cancer research. 4-(Benzyloxy)-N-benzamidoaniline is also used as a building block in the synthesis of various organic compounds due to its versatile reactivity and functional groups. Additionally, it has been studied for its potential biological and pharmacological activities, making it a highly versatile and valuable chemical compound in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 1097-35-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,9 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1097-35:
(6*1)+(5*0)+(4*9)+(3*7)+(2*3)+(1*5)=74
74 % 10 = 4
So 1097-35-4 is a valid CAS Registry Number.

1097-35-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-(4-phenylmethoxyphenyl)benzohydrazide

1.2 Other means of identification

Product number -
Other names 4'-benzyloxy-benzanilide

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:1097-35-4 SDS

1097-35-4Relevant articles and documents

Amide bond formation in aqueous solution: Direct coupling of metal carboxylate salts with ammonium salts at room temperature

Nielsen, John,Tung, Truong Thanh

supporting information, p. 10073 - 10080 (2021/12/10)

Herein, we report a green, expeditious, and practically simple protocol for direct coupling of carboxylate salts and ammonium salts under ACN/H2O conditions at room temperature without the addition of tertiary amine bases. The water-soluble coupling reagent EDC·HCl is a key component in the reaction. The reaction runs smoothly with unsubstituted/substituted ammonium salts and provides a clean product without column chromatography. Our reaction tolerates both carboxylate (which are unstable in other forms) and amine salts (which are unstable/volatile when present in free form). We believe that the reported method could be used as an alternative and suitable method at the laboratory and industrial scales. This journal is

Tetrazole NK1 receptor antagonists: The identification of an exceptionally potent orally active antiemetic compound

Armour,Chung,Congreve,Evans,Guntrip,Hubbard,Kay,Middlemiss,Mordaunt,Pegg,Vinader,Ward,Watson

, p. 1015 - 1020 (2007/10/03)

The medicinal chemistry strategy which led to the identification of GR205171, an orally active non-peptide neurokinin-1 receptor antagonist that is the most potent broad-spectrum antiemetic agent reported to date.

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