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103204-28-0

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103204-28-0 Usage

General Description

β-hydroxy-2-methoxy-benzenepropanenitrile is a chemical compound with the formula C10H11NO2. It is also known as 3-hydroxy-5-methoxybenzonitrile and is a white crystalline solid with a molecular weight of 177.20 g/mol. β-hydroxy-2-methoxy-benzenepropanenitrile has been found to have potential pharmaceutical applications, particularly in the field of drug development. It has been studied for its anti-inflammatory and antioxidant properties, as well as its potential use as a neuroprotective agent. Additionally, β-hydroxy-2-methoxy-benzenepropanenitrile has been identified as a natural product present in certain plants, where it may play a role in defense against pests or pathogens. Overall, this compound shows promise for various medicinal and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 103204-28-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,2,0 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 103204-28:
(8*1)+(7*0)+(6*3)+(5*2)+(4*0)+(3*4)+(2*2)+(1*8)=60
60 % 10 = 0
So 103204-28-0 is a valid CAS Registry Number.

103204-28-0Relevant articles and documents

Unexpected stereorecognition in nitrilase-catalyzed hydrolysis of β-hydroxy nitriles

Kamila, Sukanta,Zhu, Dunming,Biehl, Edward R.,Hua, Ling

, p. 4429 - 4431 (2006)

Biocatalytic enantioselective hydrolysis of β-hydroxy nitriles to corresponding (S)-enriched β-hydroxy carboxylic acids has been achieved for the first time by an isolated nitrilase bII6402 from Bradyrhizobium japonicum USDA110. This offers a new "green" approach to optically pure β-hydroxy nitriles and β-hydroxy carboxylic acids. The observed remote stereorecognition is surprising because this nitrilase shows no enantioselectivity for the hydrolysis of α-hydroxy nitriles such as mandelonitrile.

P(i-PrNCH2CH2)3N as a Lewis base catalyst for the synthesis of β-hydroxynitriles using TMSAN

Wadhwa, Kuldeep,Verkade, John G.

experimental part, p. 5683 - 5686 (2009/12/06)

(Equation Presented) Proazaphosphatrane 1a was found to be an efficient catalyst for synthesis of β-hydroxynitriles via the reaction of trimethylsilylacetonitrile (TMSAN) with aldehydes under mild reaction conditions and typically low catalyst loading (ca. 2 mol %). A variety of functional groups were tolerated, and good to excellent product yields were obtained.

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