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BOC-(S)-3-AMINO-5-HEXENOIC ACID is an organic compound with the molecular formula C9H15NO3. It is a derivative of amino acids, featuring a protected amino group and a hexenoic acid backbone. BOC-(S)-3-AMINO-5-HEXENOIC ACID is known for its potential applications in the synthesis of various bioactive molecules and pharmaceuticals.

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  • 270263-03-1 Structure
  • Basic information

    1. Product Name: BOC-(S)-3-AMINO-5-HEXENOIC ACID
    2. Synonyms: BOC-(S)-3-AMINO-5-HEXENOIC ACID;BOC-L-BETA-HOMOALLYLGLYCINE;BOC-ALGLY-(C*CH2)OH;BOC-BETA-HOGLY(ALLYL)-OH;N-T-BUTOXYCARBONYL-(S)-3-AMINO-5-HEXENOIC ACID;N-BETA-T-BUTOXYCARBONYL-L-HOMOALLYLGLYCINE;RARECHEM AK PT B009;Boc-b-HoGly(allyl)-OH
    3. CAS NO:270263-03-1
    4. Molecular Formula: C11H19NO4
    5. Molecular Weight: 229.27
    6. EINECS: N/A
    7. Product Categories: 3-Amino-4-phenylbutyric Acid Analogs;3-Amino-4-phenylbutanoic Acid Analogs;B-Amino
    8. Mol File: 270263-03-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 372.23 °C at 760 mmHg
    3. Flash Point: 178.919 °C
    4. Appearance: /
    5. Density: 1.078
    6. Vapor Pressure: 1.45E-06mmHg at 25°C
    7. Refractive Index: 1.472
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. PKA: 4.43±0.10(Predicted)
    11. BRN: 9127734
    12. CAS DataBase Reference: BOC-(S)-3-AMINO-5-HEXENOIC ACID(CAS DataBase Reference)
    13. NIST Chemistry Reference: BOC-(S)-3-AMINO-5-HEXENOIC ACID(270263-03-1)
    14. EPA Substance Registry System: BOC-(S)-3-AMINO-5-HEXENOIC ACID(270263-03-1)
  • Safety Data

    1. Hazard Codes: Xn
    2. Statements: 22-36/37/38
    3. Safety Statements: 26-24/25
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 270263-03-1(Hazardous Substances Data)

270263-03-1 Usage

Uses

Used in Pharmaceutical Industry:
BOC-(S)-3-AMINO-5-HEXENOIC ACID is used as a reactant for the preparation of lactam bridged peptide mimics by peptide coupling and olefin metathesis. This application is significant because lactam bridged peptide mimics are valuable in the development of novel drugs with improved stability, selectivity, and bioavailability. The compound's unique structure allows for the creation of diverse peptide-based therapeutics, which can target specific biological pathways and receptors.

Check Digit Verification of cas no

The CAS Registry Mumber 270263-03-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,0,2,6 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 270263-03:
(8*2)+(7*7)+(6*0)+(5*2)+(4*6)+(3*3)+(2*0)+(1*3)=111
111 % 10 = 1
So 270263-03-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H19NO4/c1-5-6-8(7-9(13)14)12-10(15)16-11(2,3)4/h5,8H,1,6-7H2,2-4H3,(H,12,15)(H,13,14)/t8-/m0/s1

270263-03-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (H52196)  (S)-3-(Boc-amino)-5-hexenoic acid, 95%   

  • 270263-03-1

  • 250mg

  • 1548.0CNY

  • Detail
  • Alfa Aesar

  • (H52196)  (S)-3-(Boc-amino)-5-hexenoic acid, 95%   

  • 270263-03-1

  • 1g

  • 4939.0CNY

  • Detail
  • Aldrich

  • (711950)  (S)-3-(Boc-amino)-5-hexenoicacid  98%

  • 270263-03-1

  • 711950-250MG

  • 1,470.69CNY

  • Detail

270263-03-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Boc-(S)-3-amino-5-hexenoic acid

1.2 Other means of identification

Product number -
Other names (S)-3-((tert-Butoxycarbonyl)amino)hex-5-enoic acid

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:270263-03-1 SDS

270263-03-1Downstream Products

270263-03-1Relevant articles and documents

THERAPEUTIC COMPOUNDS AND METHODS OF USE THEREOF

-

Paragraph 0212, (2019/09/06)

The invention provides a compound as described herein or a pharmaceutically acceptable salt thereof, and compositions containing such compounds and methods for using such compounds and compositions.

THERAPEUTIC COMPOUNDS AND METHODS OF USE THEREOF

-

Paragraph 0386; 0391; 0392, (2018/04/26)

The invention provides a compound of formula I: or a pharmaceutically acceptable salt thereof, wherein the variables X, Y1-Y5, R1, R2, R3, R4, and Het have the meaning as described herein, and compositions containing such compounds and methods for using such compounds and compositions.

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