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CAS

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918149-64-1

(S)-3-Phenyl-pent-4-enoic acid amide, also known as 3-Phenyl-4-aminocrotonic acid or 3-Phenyl-4-enamino acid, is an organic compound characterized by its molecular formula C11H13NO. It presents as a white to off-white powder and is recognized for its potential biological and pharmacological activities, such as anti-inflammatory and analgesic properties. Its unique structure and properties render it a valuable compound in the field of medicinal chemistry, particularly for the development of new drugs and pharmaceutical products.

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  • 918149-64-1 Structure

  • Basic information

    1. Product Name: (S)-3-PHENYL-PENT-4-ENOIC ACID AMIDE
    2. Synonyms: (S)-3-PHENYL-PENT-4-ENOIC ACID AMIDE
    3. CAS NO:918149-64-1
    4. Molecular Formula: C11H13NO
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 918149-64-1.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: (S)-3-PHENYL-PENT-4-ENOIC ACID AMIDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-3-PHENYL-PENT-4-ENOIC ACID AMIDE(918149-64-1)
    11. EPA Substance Registry System: (S)-3-PHENYL-PENT-4-ENOIC ACID AMIDE(918149-64-1)

  • 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: 918149-64-1(Hazardous Substances Data)

918149-64-1 Usage

Uses

Used in Pharmaceutical Industry:
(S)-3-Phenyl-pent-4-enoic acid amide is used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. Its versatile structure allows for the creation of a wide range of drugs with different therapeutic applications.
Used in Medicinal Chemistry:
(S)-3-Phenyl-pent-4-enoic acid amide is used as a key component in the development of new drugs and pharmaceutical products. Its anti-inflammatory and analgesic properties make it a promising candidate for the treatment of various conditions, including pain and inflammation-related disorders.
Used in Research and Development:
In the field of research and development, (S)-3-Phenyl-pent-4-enoic acid amide is utilized for studying its potential biological and pharmacological activities. This helps in understanding its mechanisms of action and identifying new therapeutic targets for drug development.
Used in Drug Design:
(S)-3-Phenyl-pent-4-enoic acid amide is employed in drug design to create novel molecular structures with improved pharmacological properties. Its unique features can be exploited to develop drugs with enhanced efficacy, selectivity, and reduced side effects.

Check Digit Verification of cas no

The CAS Registry Mumber 918149-64-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,8,1,4 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 918149-64:
(8*9)+(7*1)+(6*8)+(5*1)+(4*4)+(3*9)+(2*6)+(1*4)=191
191 % 10 = 1
So 918149-64-1 is a valid CAS Registry Number.

918149-64-1SDS

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 (S)-(-)-3-phenyl-4-pentenamide

1.2 Other means of identification

Product number -
Other names (S)-3-Phenyl-pent-4-enoic acid amide

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:918149-64-1 SDS

918149-64-1Relevant articles and documents

An unusual β-vinyl effect leading to high efficiency and enantioselectivity of the amidase, nitrile biotransformations for the preparation of enantiopure 3-arylpent-4-enoic acids and amides and their applications in synthesis

Gao, Ming,Wang, De-Xian,Zheng, Qi-Yu,Wang, Mei-Xiang

, p. 9532 - 9535 (2007/10/03)

(Chemical Equation Presented) Biotransformations of 3-arylpent-4- enenitriles catalyzed by Rhodococcus erythropolis AJ270, a nitrile hydratase/amidase-containing microbial whole-cell catalyst were studied, and an unusual β-vinyl effect of the substrate on

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