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790-48-7

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790-48-7 Usage

Usage

a. Reagent in organic synthesis
b. Raw material in pharmaceutical production
c. Raw material in agrochemical production

Chemical properties

a. Potential to act as a ligand
b. Ability to bind to metal ions

Coordination chemistry

Useful in coordination chemistry due to its ligand properties

Biological applications

a. Potential anti-inflammatory agent
b. Potential anti-bacterial agent

Safety precautions

Toxic and can cause irritation to skin, eyes, and respiratory system

Check Digit Verification of cas no

The CAS Registry Mumber 790-48-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,9 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 790-48:
(5*7)+(4*9)+(3*0)+(2*4)+(1*8)=87
87 % 10 = 7
So 790-48-7 is a valid CAS Registry Number.

790-48-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methyl-N-[(E)-(4-nitrophenyl)methylideneamino]aniline

1.2 Other means of identification

Product number -
Other names 4-nitrobenzaldehyde N-methyl-N-phenylhydrazone

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:790-48-7 SDS

790-48-7Downstream Products

790-48-7Relevant articles and documents

N-silyloxaziridines: Synthesis and use for electrophilic amination

Richy, Nicolas,Ghoraf, Mohammed,Vidal, Jo?lle

, p. 10972 - 10977 (2013/02/22)

N-Silyloxaziridines were synthesized for the first time. Their tert-butyldiphenylsilyl (TBDPS) derivatives were stable reagents that were prepared on a multigram scale in three steps and in 44% overall yield from the corresponding benzylamines. They were mild electrophilic aminating reagents that reacted at room temperature with diversely substituted primary and secondary amines to produce N-monoalkyl or N,N-dialkyl benzaldehyde hydrazones in 44a-87% yield.

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