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17547-09-0

BOC-BETA-ALA-ONP is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 17547-09-0 Structure

  • Basic information

    1. Product Name: BOC-BETA-ALA-ONP
    2. Synonyms: BOC-BETA-ALA-ONP;BOC-BETA-ALANINE 4-NITROPHENYL ESTER;Boc-b-Ala-ONp;Boc-β-alanine 4-nitrophenyl ester;4-Nitrophenyl 3-((tert-butoxycarbonyl)aMino)propanoate;N-tert-Butoxycarbonyl-beta-alanine 4-nitrophenyl ester;Boc-β-alanine 4-nitrophenyl ester≥ 97% (HPLC);Boc-2-Ala-ONp
    3. CAS NO:17547-09-0
    4. Molecular Formula: C14H18N2O6
    5. Molecular Weight: 310.3
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 17547-09-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 473 °C at 760 mmHg
    3. Flash Point: 239.9 °C
    4. Appearance: /
    5. Density: 1.239±0.06 g/cm3 (20 ºC 760 Torr)
    6. Vapor Pressure: 4.08E-09mmHg at 25°C
    7. Refractive Index: 1.529
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: BOC-BETA-ALA-ONP(CAS DataBase Reference)
    11. NIST Chemistry Reference: BOC-BETA-ALA-ONP(17547-09-0)
    12. EPA Substance Registry System: BOC-BETA-ALA-ONP(17547-09-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS:
    6. F: 8
    7. HazardClass: N/A
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 17547-09-0(Hazardous Substances Data)

17547-09-0 Usage

Chemical Properties

White to off-white powder

Check Digit Verification of cas no

The CAS Registry Mumber 17547-09-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,4 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17547-09:
(7*1)+(6*7)+(5*5)+(4*4)+(3*7)+(2*0)+(1*9)=120
120 % 10 = 0
So 17547-09-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H18N2O6/c1-14(2,3)22-13(18)15-9-8-12(17)21-11-6-4-10(5-7-11)16(19)20/h4-7H,8-9H2,1-3H3,(H,15,18)

17547-09-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-nitrophenyl) 3-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate

1.2 Other means of identification

Product number -
Other names 4-nitrophenyl 3-[[(1,1-dimethylethoxy)carbonyl]amino]propionate

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:17547-09-0 SDS

17547-09-0Relevant articles and documents

Enzymatic peptide synthesis with p-guanidinophenyl and p- (guanidinomethyl)phenyl esters as acyl donors

Sekizaki, Haruo,Itoh, Kunihiko,Toyota, Eiko,Tanizawa, Kazutaka

, p. 846 - 849 (1998)

Two series of 'inverse substrates', N-Boc-amino acid p-guanidinophenyl and p-(guanidinomethyl)phenyl esters, were prepared as acyl donor components for enzymatic peptide synthesis. The kinetic behavior of these esters toward bovine and Streptomyces griseus (SG) trypsin was analyzed. The spatial requirement of the active site of these enzymes for catalytic efficiency is discussed based on the steric characteristics of the substrates. These substrates were found to couple readily with amino acid p-nitroanilides to produce peptides. SG trypsin was the most efficient catalyst among the enzymes tested (bovine, porcine, and SG trypsin).

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