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L-phenylalanine 4-chlorobutyl ester hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 131326-15-3 Structure
  • Basic information

    1. Product Name: L-phenylalanine 4-chlorobutyl ester hydrochloride
    2. Synonyms: L-phenylalanine 4-chlorobutyl ester hydrochloride
    3. CAS NO:131326-15-3
    4. Molecular Formula:
    5. Molecular Weight: 292.205
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 131326-15-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: L-phenylalanine 4-chlorobutyl ester hydrochloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: L-phenylalanine 4-chlorobutyl ester hydrochloride(131326-15-3)
    11. EPA Substance Registry System: L-phenylalanine 4-chlorobutyl ester hydrochloride(131326-15-3)
  • 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: 131326-15-3(Hazardous Substances Data)

131326-15-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131326-15-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,3,2 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 131326-15:
(8*1)+(7*3)+(6*1)+(5*3)+(4*2)+(3*6)+(2*1)+(1*5)=83
83 % 10 = 3
So 131326-15-3 is a valid CAS Registry Number.

131326-15-3Relevant articles and documents

USE OF 4-CHLOROBUTYL ESTERS IN PEPTIDE SYNTHESIS

Trigo, M. Joaquina S. A. Amaral,Santos, M. Isabel A. Oliveira

, p. 2357 - 2359 (2007/10/02)

Ho and Wong synthesised 4-chlorobutyl esters of simple carboxylic acids and removed the ester group by the action of sodium sulfide under reflux conditions.We describe here the synthesis of the 4-chlorobutyl esters of glycine and L-phenylalanine and its use in the synthesis of six new N-protected dipeptides 4-chlorobutyl esters (XHNCH2CO-HNCHRCO2(CH2)4Cl; R = H, CH2Ph; X = Z, Boc, Trt).The selective removal of the 4-chlorobutyl group can be achieved by the action of the sulfide anion in aqueous acetonitrile (room temperature, 1.5 to 5 h).The conditions are milder than those described, but similar to the conditions used with the dipeptides 2-bromoethyl esters.The N-protected dipeptides were isolated in 50 to 80percent yield.

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