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Alloisoleucine, 2-methyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 106292-42-6 Structure
  • Basic information

    1. Product Name: Alloisoleucine, 2-methyl- (9CI)
    2. Synonyms: Alloisoleucine, 2-methyl- (9CI)
    3. CAS NO:106292-42-6
    4. Molecular Formula: C7H15NO2
    5. Molecular Weight: 145.1995
    6. EINECS: N/A
    7. Product Categories: GLYCINESCAFFOLD
    8. Mol File: 106292-42-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Alloisoleucine, 2-methyl- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Alloisoleucine, 2-methyl- (9CI)(106292-42-6)
    11. EPA Substance Registry System: Alloisoleucine, 2-methyl- (9CI)(106292-42-6)
  • 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: 106292-42-6(Hazardous Substances Data)

106292-42-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106292-42-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,2,9 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 106292-42:
(8*1)+(7*0)+(6*6)+(5*2)+(4*9)+(3*2)+(2*4)+(1*2)=106
106 % 10 = 6
So 106292-42-6 is a valid CAS Registry Number.

106292-42-6Downstream Products

106292-42-6Relevant articles and documents

MASP INHIBITORY COMPOUNDS AND USES THEREOF

-

, (2020/11/23)

The present invention relates to novel Mannose-binding lectin (MBL)-associated serine protease (MASP) inhibitory compounds, as well as analogues and derivatives thereof, to processes for the preparation thereof, to the use thereof alone or in combinations for treatment and/or prevention of diseases and to the use thereof for production of medicaments for treatment and/or prevention of diseases, especially for treatment and/or prevention of renal and cardiovascular disorders and of ischemia reperfusion injuries.

Enantioselective synthesis and enantiomeric amplification of amino acids under prebiotic conditions

Levine, Mindy,Kenesky, Craig Scott,Mazori, Daniel,Breslow, Ronald

supporting information; experimental part, p. 2433 - 2436 (2009/05/27)

(Chemical Equation Presented) A plausible origin of biomolecular homochirality is advanced, where α-methyl amino acids found on meteorites transfer their chirality in the synthesis of normal amino acids. This asymmetry can be amplified to nearly homochiral levels, thus providing the necessary prerequisite for life to start on this planet and elsewhere in the universe.

Process for preparation of alpha-alkyl amino acids

-

, (2008/06/13)

A process for preparing α-alkyl amino acids by enantioretentive α-alkylation of α-amino acids is described. The products are bioactive compounds including some useful as therapeutic agents.

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