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Benzenemethanol, 4-(dimethylamino)-a-ethynyl-a-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

118965-01-8

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118965-01-8 Usage

Chemical compound

Benzenemethanol, 4-(dimethylamino)-a-ethynyl-a-phenyl-

Also known as

DMHP

Class

Synthetic opioids

Properties

Psychoactive, potent analgesic effect, euphoric and sedative effects

Use

Recreational purposes

Regulation

Controlled substance in many countries

Medicinal potential

Studied for pain-relieving properties

Unregulated use

Associated with significant health risks

Check Digit Verification of cas no

The CAS Registry Mumber 118965-01-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,9,6 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 118965-01:
(8*1)+(7*1)+(6*8)+(5*9)+(4*6)+(3*5)+(2*0)+(1*1)=148
148 % 10 = 8
So 118965-01-8 is a valid CAS Registry Number.

118965-01-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-dimethylaminophenyl)-1-phenyl-2-propyn-1-ol

1.2 Other means of identification

Product number -
Other names 1-(p-dimethylaminophenyl)-1-phenyl-2-propyn-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:118965-01-8 SDS

118965-01-8Downstream Products

118965-01-8Relevant academic research and scientific papers

Synthesis and photochromic behaviour of a series of benzopyrans bearing an: N -phenyl-carbazole moiety: Photochromism control by the steric effect

Adachi, Chihaya,Frigoli, Michel,Jousselin-Oba, Tanguy,Mamada, Masashi,Marrot, Jér?me,Ortica, Fausto,Pannacci, Danilo,Zangarelli, Agnese

, p. 1344 - 1355 (2020)

Five new N-phenyl-carbazole benzopyrans bearing different substitutions on one of the phenyl rings at the sp3 carbon have been synthesized. Their molecular structures were investigated by X-ray and NMR analyses and through quantum chemical calculations. T

Photochromic naphthopyrans

-

, (2008/06/13)

Described are novel reversible photochromic naphthopyran compounds substituted at the number eight carbon atom on the naphtho portion of the naphthopyran ring with, for example, a methoxy group. Also described are polymeric organic host materials that con

Photochromic naphthopyrans

-

, (2008/06/13)

Described are novel reversible photochromic naphthopyran compounds substituted at the number eight carbon atom on the naphtho portion of the naphthopyran ring with, for example, a methoxy group. Also described are organic host materials that contain or th

A Simple and Convenient Synthesis of Aryl-Substituted Push-Pull Butadienes from 1,1-Diaryl-2-propyn-1-ols

Nakatsuji, Shin'inchi,Nakashima, Kenichiro,Iyoda, Masahiko,Akiyama, Shuzo

, p. 2253 - 2255 (2007/10/02)

1,1-Diaryl-2-propyn-1-ol derivatives reacted with several nucleophiles to afford novel 1,1-diarylbutadiene systems.An efficient one-step synthesis of aryl-substituted push-pull butadiene systems was achieved by this reaction.

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