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118970-43-7

Butanenitrile, 3-[bis(phenylmethyl)amino]-2-hydroxy-, (2S,3S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 118970-43-7 Structure

  • Basic information

    1. Product Name: Butanenitrile, 3-[bis(phenylmethyl)amino]-2-hydroxy-, (2S,3S)-
    2. Synonyms:
    3. CAS NO:118970-43-7
    4. Molecular Formula: C18H20N2O
    5. Molecular Weight: 280.37
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 118970-43-7.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: Butanenitrile, 3-[bis(phenylmethyl)amino]-2-hydroxy-, (2S,3S)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Butanenitrile, 3-[bis(phenylmethyl)amino]-2-hydroxy-, (2S,3S)-(118970-43-7)
    11. EPA Substance Registry System: Butanenitrile, 3-[bis(phenylmethyl)amino]-2-hydroxy-, (2S,3S)-(118970-43-7)

  • 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: 118970-43-7(Hazardous Substances Data)

118970-43-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 118970-43-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,9,7 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 118970-43:
(8*1)+(7*1)+(6*8)+(5*9)+(4*7)+(3*0)+(2*4)+(1*3)=147
147 % 10 = 7
So 118970-43-7 is a valid CAS Registry Number.

118970-43-7Relevant articles and documents

STEREOSELECTIVE CYANOHYDRIN-FORMING REACTIONS OF CHIRAL α-AMINO ALDEHYDES

Reetz, M. T.,Drewes, M. W.,Harms, K.,Reif, W.

, p. 3295 - 3298 (1988)

The Lewis acid mediated cyanohydrin-forming addition of Me3SiCN to optically active α-dibenzylamino aldehydes 2 occurs stereoselectively.Chelation controlled adducts 3 result if MgBr2 or TiCl4 is used, whereas the diastereomers 4 are obtained upon employi

Stereoselective cyanation of chiral α-amino aldehydes by reaction with Nagata's reagent: A route to enantiopure β-amino-α-hydroxy acids

Andres, Jose M.,Martinez, Maria A.,Pedrosa, Rafael,Perez-Encabo, Alfonso

, p. 347 - 353 (2007/10/03)

Chiral α-dibenzylamino aldehydes react with diethylaluminum cyanide leading to anti-β-dibenzylamino-α-hydroxycyanides as the major diastereoisomers in good yields and diastereomeric excesses. Hydrolysis of the nitrile derivatives allows the synthesis of enantiopure β-amino-α-hydroxy acids.

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