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CAS

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90376-98-0

(R)-ALPHA-METHYLVALINAMIDE is an organic compound that belongs to the class of amides, characterized by the replacement of the carboxyl group, COOH, with a carboxamide group, CONR2. The "R" in its name signifies the configuration of the chiral center, which is an important aspect of its orientation. The term "Alpha-Methylvalinamide" refers to the specific structural components of the compound, including the Alpha-Methylvaline molecule and the amide functional group attached to it. This chemical is valuable for its use in various biological studies and chemical reactions.

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  • 90376-98-0 Structure

  • Basic information

    1. Product Name: (R)-ALPHA-METHYLVALINAMIDE
    2. Synonyms: (R)-ALPHA-METHYLVALINAMIDE
    3. CAS NO:90376-98-0
    4. Molecular Formula: C6H14N2O
    5. Molecular Weight: 130.19
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 90376-98-0.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: (R)-ALPHA-METHYLVALINAMIDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-ALPHA-METHYLVALINAMIDE(90376-98-0)
    11. EPA Substance Registry System: (R)-ALPHA-METHYLVALINAMIDE(90376-98-0)

  • 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: 90376-98-0(Hazardous Substances Data)

90376-98-0 Usage

Uses

Used in Pharmaceutical Industry:
(R)-ALPHA-METHYLVALINAMIDE is used as an intermediate in the synthesis of pharmaceutical compounds for its unique structural properties and reactivity, contributing to the development of new drugs with potential therapeutic applications.
Used in Chemical Research:
(R)-ALPHA-METHYLVALINAMIDE is utilized as a research chemical in various chemical studies, allowing scientists to explore its properties, reactivity, and potential applications in the synthesis of other organic compounds.
Used in Biochemical Applications:
(R)-ALPHA-METHYLVALINAMIDE is employed in biochemical research to investigate its interactions with biological systems, potentially leading to insights into its role in biological processes and the development of bioactive molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 90376-98-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,7 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 90376-98:
(7*9)+(6*0)+(5*3)+(4*7)+(3*6)+(2*9)+(1*8)=150
150 % 10 = 0
So 90376-98-0 is a valid CAS Registry Number.

90376-98-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-α-METHYLVALINAMIDE

1.2 Other means of identification

Product number -
Other names Lopac-M-8131

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:90376-98-0 SDS

90376-98-0Relevant articles and documents

Synthesis of dipeptides containing α-substituted amino acids; their use as chiral ligands in Lewis-acid-catalyzed reactions

Kaptein, Bernard,Monaco, Vania,Broxterman, Quirinus B.,Schoemaker, Hans E.,Kamphuis, Johan

, p. 231 - 238 (2007/10/02)

L-α-Methylphenylalanine, obtained by enzymatic resolution of the corresponding racemic amide with amidase from Ochrobactrum anthropi NCIMB 40321, was used in the synthesis of dipeptides containing α-substituted amino acids.The 2-hydroxynaphthalene-1-carboxaldehyde Schiff bases of the dipeptides (1 and 2) were tested as Ti(IV) and Al(III) complexes in asymmetric Lewis-acid-catalyzed reactions.Only the Al(III) complex of 2 showed moderate enantioselectivity in the cyanation reaction of benzaldehyde with TMS-CN.

Synthesis of Optically Pure α-Alkylated α-Amino Acids and a Single-Step Method for Enatiomeric Excess Determination

Kruizinga, Wim H.,Bolster, John,Kellogg, Richard M.,Kamphuis, Johan,Boesten, Wilhelmus H. J.,et al.

, p. 1826 - 1827 (2007/10/02)

A method for the enzymatic resolution of the amides of some racemic α-alkylated amino acids is described as well as a method involving derivatization with (S)-2-chloropropionyl chloride followed by 1H NMR analysis to establish the enantiomeric excesses of the free amino acids.

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