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CAS

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1261297-83-9

(S)-2-(2-(1-hydroxy-3-phenylprop-2-yl)-2-isopropylhydrazinecarbonyl)-6-methylphenyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1261297-83-9 Structure

  • Basic information

    1. Product Name: (S)-2-(2-(1-hydroxy-3-phenylprop-2-yl)-2-isopropylhydrazinecarbonyl)-6-methylphenyl acetate
    2. Synonyms:
    3. CAS NO:1261297-83-9
    4. Molecular Formula:
    5. Molecular Weight: 384.475
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1261297-83-9.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: (S)-2-(2-(1-hydroxy-3-phenylprop-2-yl)-2-isopropylhydrazinecarbonyl)-6-methylphenyl acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-2-(2-(1-hydroxy-3-phenylprop-2-yl)-2-isopropylhydrazinecarbonyl)-6-methylphenyl acetate(1261297-83-9)
    11. EPA Substance Registry System: (S)-2-(2-(1-hydroxy-3-phenylprop-2-yl)-2-isopropylhydrazinecarbonyl)-6-methylphenyl acetate(1261297-83-9)

  • 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: 1261297-83-9(Hazardous Substances Data)

1261297-83-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1261297-83-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,1,2,9 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1261297-83:
(9*1)+(8*2)+(7*6)+(6*1)+(5*2)+(4*9)+(3*7)+(2*8)+(1*3)=159
159 % 10 = 9
So 1261297-83-9 is a valid CAS Registry Number.

1261297-83-9Relevant articles and documents

Synthesis and application of oxadiazines as chiral ligands for the enantioselective addition of diethylzinc to aldehydes

Dean, Melissa A.,Hitchcock, Shawn R.

, p. 2471 - 2478 (2010)

A series of oxadiazines derived from l-phenylalanine bearing phenolic substituents have been synthesized in a multistep, one pot process. This process involves the reaction of a mixed anhydride with a β-hydrazino alcohol, methanesulfonylation of the alcohol moiety, and base induced cyclization. The resultant oxadiazines were employed in the asymmetric addition of diethylzinc to aldehydes.

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