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103205-23-8

3-hjydroxy-3-(3-methoxyphenyl)propanenitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 103205-23-8 Structure

  • Basic information

    1. Product Name: 3-hjydroxy-3-(3-methoxyphenyl)propanenitrile
    2. Synonyms: 3-hjydroxy-3-(3-methoxyphenyl)propanenitrile
    3. CAS NO:103205-23-8
    4. Molecular Formula:
    5. Molecular Weight: 177.203
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 103205-23-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-hjydroxy-3-(3-methoxyphenyl)propanenitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-hjydroxy-3-(3-methoxyphenyl)propanenitrile(103205-23-8)
    11. EPA Substance Registry System: 3-hjydroxy-3-(3-methoxyphenyl)propanenitrile(103205-23-8)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 103205-23-8(Hazardous Substances Data)

103205-23-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103205-23-8 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 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 103205-23:
(8*1)+(7*0)+(6*3)+(5*2)+(4*0)+(3*5)+(2*2)+(1*3)=58
58 % 10 = 8
So 103205-23-8 is a valid CAS Registry Number.

103205-23-8Relevant articles and documents

Zinc-mediated addition of bromoacetonitrile to carbonyl compounds under solvent-free conditions

Zhang, Yumei,Du, Xi,An, Bin

, p. 73 - 75 (2014)

Zinc mediated addition reaction of bromoacetonitrile with aryl aldehydes and ketones produces β-hydroxynitriles under solvent-free conditions. The valuable feature of the methodology are solvent-free and catalyst-free conditions and short reaction times (5 min).

Catalytic nucleophilic activation of acetonitrile via a cooperative catalysis of cationic Ru complex, DBU, and NaPF6

Kumagai, Naoya,Matsunaga, Shigeki,Shibasaki, Masakatsu

, p. 8598 - 8608 (2008/02/10)

The development of an efficient catalytic system for the direct addition of acetonitrile under mild amine basic conditions is described. A cooperative catalysis of CpRu complex, DBU, and NaPF6 enables chemoselective and catalytic generation of

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

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

, p. 4429 - 4431 (2007/10/03)

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.

Cooperative catalysis of a cationic ruthenium complex, amine base, and Na salt: Catalytic activation of acetonitrile as a nucleophile

Kumagai, Naoya,Matsunaga, Shigeki,Shibasaki, Masakatsu

, p. 13632 - 13633 (2007/10/03)

Cooperative catalysis of a cationic Ru complex, DBU, and NaPF6 is described. An exquisite combination of the catalytic triad enabled catalytic activation of acetonitrile as a nucleophile under mild amine-basic conditions. Addition of in situ-ge

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