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42389-54-8

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42389-54-8 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 68, p. 1296, 1946 DOI: 10.1021/ja01211a053

Check Digit Verification of cas no

The CAS Registry Mumber 42389-54-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,3,8 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 42389-54:
(7*4)+(6*2)+(5*3)+(4*8)+(3*9)+(2*5)+(1*4)=128
128 % 10 = 8
So 42389-54-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H22N2/c1-3-12(4-2)10-7-5-9(11)6-8-10/h9-10H,3-8,11H2,1-2H3

42389-54-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Amino-4-(diethylamino)cyclohexane

1.2 Other means of identification

Product number -
Other names N,N-Diethyl-1,4-cyclohexanediamine

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:42389-54-8 SDS

42389-54-8Relevant articles and documents

Novel isoxazole carboxamides as growth hormone secretagogue receptor (GHS-R) antagonists

Liu, Bo,Liu, Gang,Xin, Zhili,Serby, Micheal D.,Zhao, Hongyu,Schaefer, Verlyn G.,Falls, H. Douglas,Kaszubska, Wiweka,Collins, Christine A.,Sham, Hing L.

, p. 5223 - 5226 (2007/10/03)

Novel isoxazole carboxamides have been identified as growth hormone secretagogue receptor (GHS-R) antagonists. Substituent modification off the 5-position of the isoxazole ring led to analogues with potent binding affinity and functional antagonism of GHS-R. A potent analogue (32) with high aqueous solubility and good GPCR selectivity was also identified as a potential pharmacological tool for in vivo studies.

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