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(S)-3-methyl-2-((S)-1-phenylethylamino)butan-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1010385-10-0 Structure
  • Basic information

    1. Product Name: (S)-3-methyl-2-((S)-1-phenylethylamino)butan-1-ol
    2. Synonyms: (S)-3-methyl-2-((S)-1-phenylethylamino)butan-1-ol
    3. CAS NO:1010385-10-0
    4. Molecular Formula:
    5. Molecular Weight: 207.316
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1010385-10-0.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)-3-methyl-2-((S)-1-phenylethylamino)butan-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-3-methyl-2-((S)-1-phenylethylamino)butan-1-ol(1010385-10-0)
    11. EPA Substance Registry System: (S)-3-methyl-2-((S)-1-phenylethylamino)butan-1-ol(1010385-10-0)
  • 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: 1010385-10-0(Hazardous Substances Data)

1010385-10-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1010385-10-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,0,3,8 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1010385-10:
(9*1)+(8*0)+(7*1)+(6*0)+(5*3)+(4*8)+(3*5)+(2*1)+(1*0)=80
80 % 10 = 0
So 1010385-10-0 is a valid CAS Registry Number.

1010385-10-0Downstream Products

1010385-10-0Relevant articles and documents

Alternative and complementary approaches to the asymmetric synthesis of C3 substituted NH free or N-substituted isoindolin-1-ones

Lamblin, Marc,Couture, Axel,Deniau, Eric,Grandclaudon, Pierre

, p. 111 - 123 (2008/09/17)

Complementary synthetic approaches to enantiomerically pure C3 alkylated or arylated NH free or N-substituted isoindolinones have been developed. The key step is elaboration of diversely substituted 2-alkyl- and arylbenzylamines, which can be submitted to a bis-metallation process followed by interception with a carbonylating agent. They can be also converted into N-alkylbromobenzylcarbamates or into bromobenzyldicarbamates and the assembly of the titled compounds can be readily ensured by reliance upon the Parham cyclization process.

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