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5700-56-1

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5700-56-1 Usage

General Description

1-Phenyl-Ethane-1,2-Diamine is a chemical compound that falls under the category of aliphatic amines and it is used predominantly as an organic intermediate in the production of pharmaceuticals, agrochemicals, and dyestuffs. Its molecular formula is C8H12N2 and its molecular weight is 136.193 g/mol. 1-PHENYL-ETHANE-1,2-DIAMINE is characterized by its clear colorless to light yellow liquid form at standard temperature and pressure. It possesses moderately strong basic properties. Moreover, it is slightly soluble in water and other polar solvents. Caution is advised while handling this chemical as it can cause skin and eye irritation upon contact, respiratory irritation upon inhalation, and may be harmful if swallowed.

Check Digit Verification of cas no

The CAS Registry Mumber 5700-56-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,0 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5700-56:
(6*5)+(5*7)+(4*0)+(3*0)+(2*5)+(1*6)=81
81 % 10 = 1
So 5700-56-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H12N2/c9-6-8(10)7-4-2-1-3-5-7/h1-5,8H,6,9-10H2

5700-56-1SDS

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-Phenylethane-1,2-diamine

1.2 Other means of identification

Product number -
Other names 1-phenylethane-1,2-diamine

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:5700-56-1 SDS

5700-56-1Relevant articles and documents

Palladium-Catalyzed Intermolecular Oxidative Diazidation of Alkenes

Peng, Haihui,Yuan, Zheliang,Chen, Pinhong,Liu, Guosheng

supporting information, p. 876 - 880 (2017/06/27)

A palladium-catalyzed oxidative vicinal diazidation of alkenes has been developed, in which TMSN3 was used as azide source. Both styrenes and unactivated alkenes are suitable for this reaction. And trans-alkyldiazides were obtained as major products from cyclic alkenes with moderate to good diastereoselectivities. This reaction afforded an efficient way for the synthesis of useful 1,2-diamines after hydrogenation.

One-pot protocol to synthesize N-(β-nitro)amides by tandem Henry/Ritter reaction

Ai, Wensi,Shi, Ronghua,Zhu, Liyan,Jiang, Dehong,Ma, Xiaobo,Yuan, Jilan,Wang, Zhouyu

, p. 24044 - 24048 (2015/03/30)

A novel, efficient and atom economical one pot protocol for the synthesis of N-(β-nitro)amides has been described by combining the Henry reaction with the Ritter reaction. The designed products could be obtained from easily available aldehydes, nitroalkan

COMPOUNDS, THEIR PHARMACEUTICAL COMPOSITIONS AND THEIR USES AS IDH1 MUTANTS INHIBITORS FOR TREATING CANCERS

-

, (2013/02/28)

Provided are compounds of formula (I), wherein X, Y, Z, W, V, R2, R3 and m are defined as in the description. Their pharmaceutical compositions and their uses as IDH1 mutants inhibitors for treating cancers are also provided

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