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Piperazine, 1-cyclohexyl-4-[(1R)-1,2-diphenylethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57377-70-5

57377-70-5 Suppliers

This product is a nationally controlled contraband or patented product, and the Lookchem platform doesn't provide relevant sales information.

57377-70-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57377-70-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,3,7 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 57377-70:
(7*5)+(6*7)+(5*3)+(4*7)+(3*7)+(2*7)+(1*0)=155
155 % 10 = 5
So 57377-70-5 is a valid CAS Registry Number.

57377-70-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-(-)-1-cyclohexyl-4-(1,2-diphenylethyl)piperazine

1.2 Other means of identification

Product number -
Other names 1-Cyclohexyl-4-((R)-1,2-diphenyl-ethyl)-piperazine

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:57377-70-5 SDS

57377-70-5Downstream Products

57377-70-5Relevant academic research and scientific papers

Synthesis and structure-activity relationships of 1-substituted 4-(1,2-diphenylethyl)piperazine derivatives having narcotic agonist and antagonist activity

Natsuka,Nakamura,Nishikawa,Negoro,Uno,Nishimura

, p. 1779 - 1787 (2007/10/02)

Racemates and enantiomers of 1-substituted 4-[2-(3-hydroxyphenyl)-1-phenylethyl]piperazine derivatives (3-18) were synthesized, and their analgesic and other pharmacological activities and structure-activity relationships were investigated. The S-(+) enan