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864424-01-1

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864424-01-1 Usage

Structure

Piperidine derivative with a piperidine ring, bromophenyl group, and an ethyl chain

Appearance

White powder

Solubility

Soluble in organic solvents such as ethanol and methanol

Research use

Building block for the synthesis of other organic compounds

Potential applications

Pharmaceutical applications (further research needed)

Safety

Further research needed to understand potential uses and effects

Check Digit Verification of cas no

The CAS Registry Mumber 864424-01-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,4,4,2 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 864424-01:
(8*8)+(7*6)+(6*4)+(5*4)+(4*2)+(3*4)+(2*0)+(1*1)=171
171 % 10 = 1
So 864424-01-1 is a valid CAS Registry Number.

864424-01-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[2-(2-BROMOPHENOXY)ETHYL]-PIPERIDINE

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:864424-01-1 SDS

864424-01-1Downstream Products

864424-01-1Relevant articles and documents

Synthesis of tetracyclic heterocompounds as selective estrogen receptor modulators. Part 2. Process improvement for scale-up of 2,5,8-substituted 11,12-dihydro-5H-6,13-dioxabenzo[3,4]cyclohepta-[1,2-a]naphthalene derivatives

Li, Xun,Reuman, Michael,Russell, Ronald K.,Youells, Scott,Beish, Sandra,Hu, Zhiyong,Branum, Shawn,Jain, Nareshkumar,Sui, Zhihua

, p. 731 - 738 (2007)

An improved, reproducible nonchromatographic process for scale-up synthesis of 2,5,8-substituted 11,12-dihydro-5H-6,13-dioxabenzo[3,4]cyclohepta[1,2-a] naphthalene derivatives as selective estrogen receptor modulators (SERMs) is described. The titled comp

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