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20498-65-1

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20498-65-1 Usage

Chemical structure

A phenyl group attached to a chlorophenyl group and a hydroxyl group on a two-carbon chain.

Classification

Synthetic opioid

Mechanism of action

Acts as an agonist at the μ-opioid receptor

Potency

Potent analgesic

Duration of action

Long-acting

Use

Research settings as an alternative to traditional opioids

Side effects

Respiratory depression and sedation

Potential for abuse

High potential for abuse and dependence

Regulation

Use is heavily regulated in many countries due to its potential for misuse and addiction.

Check Digit Verification of cas no

The CAS Registry Mumber 20498-65-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,4,9 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 20498-65:
(7*2)+(6*0)+(5*4)+(4*9)+(3*8)+(2*6)+(1*5)=111
111 % 10 = 1
So 20498-65-1 is a valid CAS Registry Number.

20498-65-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-chlorophenyl)-2-phenylethanol

1.2 Other means of identification

Product number -
Other names 1-(3-Chlorophenyl)-2-phenylethan-1-ol

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:20498-65-1 SDS

20498-65-1Relevant articles and documents

Chemoselective Benzylation of Aldehydes Using Lewis Base Activated Boronate Nucleophiles

Hollerbach, Michael R.,Barker, Timothy J.

, p. 1425 - 1427 (2018/05/24)

A benzylation of aldehydes using primary and secondary benzylboronic acid pinacol esters is reported. Activation of the boronic ester with s-butyllithium rendered it nucleophilic toward aldehydes. The activated nucleophile chemoselectively transfers the benzyl group over the sec-butyl group, providing excellent yields of the benzylated products. 11B NMR experiments were performed to study the mechanism of this transformation.

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