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β-Cyano-m-hydroxypropiophenone, also known as β-CHP, is a chemical compound with the molecular formula C10H8NO2. It is a derivative of propiophenone, featuring a cyano group (-CN) at the β-position and a hydroxy group (-OH) at the meta-position relative to the carbonyl group. This white crystalline substance is used as a reagent in the synthesis of various pharmaceuticals and other organic compounds. Due to its potential use in the illicit synthesis of drugs, β-CHP is a controlled substance in many countries. It is important to handle this chemical with care, as it can be hazardous and is subject to regulatory oversight.

76106-46-2

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76106-46-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76106-46-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,1,0 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 76106-46:
(7*7)+(6*6)+(5*1)+(4*0)+(3*6)+(2*4)+(1*6)=122
122 % 10 = 2
So 76106-46-2 is a valid CAS Registry Number.

76106-46-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name β-cyano-m-hydroxypropiophenone

1.2 Other means of identification

Product number -
Other names 4-(3-hydroxy-phenyl)-4-oxo-butyronitrile

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:76106-46-2 SDS

76106-46-2Relevant academic research and scientific papers

Intramolecular Alkylation of Phenols. Part 4. Base-catalysed Cyclisation of Phenolic Enones. Scope and Limitations

Murphy, William S.,Wattanasin, Sompong

, p. 1555 - 1566 (2007/10/02)

The phenolic enones (4), (5), (8), (9), and (13) cyclise readily under acidic conditions.However, neither these nor the thio-substituted phenols (11a), (13a), (14a), and (15a) closed under basic conditions.Involvement of unfavourable equilibria is disproved.Comparison is made with related successful cyclisations of the saturated ketone (38) and aldehyde (39).Preliminary results suggest that strict stereo-electronic requirements are necessary for enone ring closure and that these conditions are not met in base-catalysed 5-Endo- and 6-Endo-Trigonal ring closures of the phenols of general type (2; n=0 and n=1).

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