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14066-73-0

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14066-73-0 Usage

Physical state

Yellow solid at room temperature

Usage

Commonly used as a catalyst in organic chemical reactions

Specific applications

Preparation of natural products and pharmaceuticals

Potential application

Anti-tumor agent

Apoptosis induction

Ability to induce apoptosis in cancer cells

Industrial use

Production of semiconductors and photoelectron materials

Chemical structure

Contains a hydrazine group

Reaction potential

Potential for forming complex compounds and reactions with various functional groups

Field of application

Diverse applications in the field of organic chemistry and pharmaceuticals

Check Digit Verification of cas no

The CAS Registry Mumber 14066-73-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,6 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 14066-73:
(7*1)+(6*4)+(5*0)+(4*6)+(3*6)+(2*7)+(1*3)=90
90 % 10 = 0
So 14066-73-0 is a valid CAS Registry Number.

14066-73-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (benzhydrylideneamino)urea

1.2 Other means of identification

Product number -
Other names Semicarbazon des Benzophenons

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:14066-73-0 SDS

14066-73-0Relevant articles and documents

Solid-phase synthesis of C-terminal azapeptides

Doan, Ngoc-Duc,Zhang, Jinqiang,Traoré, Mariam,Kamdem, Winnie,Lubell, William D.

, p. 387 - 391 (2015/05/13)

The solid-phase synthesis of azapeptides possessing a C-terminal aza-residue has been accomplished by a protocol featuring regioselective alkylation of benzhydrylidene-aza-glycinamide and illustrated by the syntheses of [aza-Lys6] growth-hormone-releasing peptide-6 analogs.

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