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1-Butanone, 4-[[4-(hydroxymethyl)-4-phenylcyclohexyl]amino]-1-phenyl-, cis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56326-87-5

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56326-87-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56326-87-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,3,2 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 56326-87:
(7*5)+(6*6)+(5*3)+(4*2)+(3*6)+(2*8)+(1*7)=135
135 % 10 = 5
So 56326-87-5 is a valid CAS Registry Number.

56326-87-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-Hydroxymethyl-4-phenyl-cyclohexylamino)-1-phenyl-butan-1-one

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:56326-87-5 SDS

56326-87-5Downstream Products

56326-87-5Relevant academic research and scientific papers

Butyrophenones as hypotensive agents. Derivatives of 4 aryl 4 (hydroxymethyl)cyclohexylamine

Lednicer,Emmert,Rudzik,Graham

, p. 593 - 599 (2007/10/06)

The preparation of butyrophenone derivatives of 4 aryl 4 (hydroxymethyl) cyclohex 1 ylamines starting from the corresponding 4 cyano 4 phenylcyclohexan 1 ones is described. Substitution was varied in both rings; both isomers of 4 phenyl 4 (hydroxymethyl)cyclohex 1 ylamine were characterized. Those derivatives which carried p fluoro substitution on the butyrophenone exhibited hypotensive activity in the rat with diminished CNS activity compared to compounds lacking the hydroxymethyl group. The effect of substitution on the 4 aryl ring is discussed.

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