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55930-29-5

2-BUTYRYL AMINO PROPIONIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 55930-29-5 Structure

  • Basic information

    1. Product Name: 2-BUTYRYL AMINO PROPIONIC ACID
    2. Synonyms: 2-BUTYRYL AMINO PROPIONIC ACID;L-Alanine, N-(1-oxobutyl)-
    3. CAS NO:55930-29-5
    4. Molecular Formula: C7H13NO3
    5. Molecular Weight: 159.18
    6. EINECS: 1312995-182-4
    7. Product Categories: Erectile Dysfunction
    8. Mol File: 55930-29-5.mol
    9. Article Data: 2

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 371.8 °C at 760 mmHg
    3. Flash Point: 178.7 °C
    4. Appearance: /
    5. Density: 1.097 g/cm3
    6. Vapor Pressure: 1.5E-06mmHg at 25°C
    7. Refractive Index: 1.458
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-BUTYRYL AMINO PROPIONIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-BUTYRYL AMINO PROPIONIC ACID(55930-29-5)
    12. EPA Substance Registry System: 2-BUTYRYL AMINO PROPIONIC ACID(55930-29-5)

  • 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: 55930-29-5(Hazardous Substances Data)

55930-29-5 Usage

Chemical Properties

white powder

Check Digit Verification of cas no

The CAS Registry Mumber 55930-29-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,9,3 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 55930-29:
(7*5)+(6*5)+(5*9)+(4*3)+(3*0)+(2*2)+(1*9)=135
135 % 10 = 5
So 55930-29-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H13NO3/c1-3-4-6(9)8-5(2)7(10)11/h5H,3-4H2,1-2H3,(H,8,9)(H,10,11)

55930-29-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-BUTYRYL AMINO PROPIONIC ACID

1.2 Other means of identification

Product number -
Other names L-Alanine,N-(1-oxobutyl)

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:55930-29-5 SDS

55930-29-5Relevant articles and documents

Repurposing the 3-Isocyanobutanoic Acid Adenylation Enzyme SfaB for Versatile Amidation and Thioesterification

Zhu, Mengyi,Wang, Lijuan,He, Jing

supporting information, p. 2030 - 2035 (2020/11/30)

Genome mining of microbial natural products enables chemists not only to discover the bioactive molecules with novel skeletons, but also to identify the enzymes that catalyze diverse chemical reactions. Exploring the substrate promiscuity and catalytic mechanism of those biosynthetic enzymes facilitates the development of potential biocatalysts. SfaB is an acyl adenylate-forming enzyme that adenylates a unique building block, 3-isocyanobutanoic acid, in the biosynthetic pathway of the diisonitrile natural product SF2768 produced by Streptomyces thioluteus, and this AMP-ligase was demonstrated to accept a broad range of short-chain fatty acids (SCFAs). Herein, we repurpose SfaB to catalyze amidation or thioesterification between those SCFAs and various amine or thiol nucleophiles, thereby providing an alternative enzymatic approach to prepare the corresponding amides and thioesters in vitro.

Towards an efficient prodrug of the alkylating metabolite monomethyltriazene: Synthesis and stability of N-acylamino acid derivatives of triazenes

Perry, Maria de Jesus,Carvalho, Emilia,Rosa, Eduarda,Iley, Jim

experimental part, p. 1049 - 1056 (2009/08/14)

A series of 3-[α-(acylamino)acyl]-1-aryl-3-methyltriazenes 6a-l, potential cytotoxic triazene prodrugs, were synthesised by coupling 1-aryl-3-methyltriazenes to N-acylamino acids. Their hydrolysis was studied in isotonic pH 7.4 phosphate buffer and in hum

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