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7505-44-4

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7505-44-4 Usage

Type of compound

Urea derivative

Structural feature

Two 3-nitrophenylmethylideneamino groups attached to the nitrogen atom

Common use

Reagent in organic synthesis

Building block

Preparation of various organic compounds

Potential applications

Pharmaceuticals, agrochemicals, and material science

Studied properties

Antimicrobial and anticancer properties

Synthesis

Novel biologically active compounds

Safety precautions

Handle with caution due to potential health hazards

Hazardous exposure

May be harmful if ingested, inhaled, or comes into contact with the skin

Check Digit Verification of cas no

The CAS Registry Mumber 7505-44-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,0 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7505-44:
(6*7)+(5*5)+(4*0)+(3*5)+(2*4)+(1*4)=94
94 % 10 = 4
So 7505-44-4 is a valid CAS Registry Number.

7505-44-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(Z)-(3-nitrophenyl)methylideneamino]-3-[(E)-(3-nitrophenyl)methylideneamino]urea

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:7505-44-4 SDS

7505-44-4Downstream Products

7505-44-4Relevant articles and documents

Efficient synthesis of 1,5-disubstituted carbohydrazones using K 2CO3 as a carbonyl donor

Wen, Jun,Yang, Chu-Ting,Jiang, Tao,Hu, Sheng,Yang, Tong-Zai,Wang, Xiao-Lin

supporting information, p. 2398 - 2401 (2014/05/20)

A novel reaction that generates 1,5-disubstituted carbohydrazones via the carbonylation of tosylhydrazones has been developed. For the first time, the inexpensive, readily available, environmentally friendly, and nongaseous potassium carbonate is used as

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