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63250-32-8

SUC-PRO-OH is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 63250-32-8 Structure

  • Basic information

    1. Product Name: SUC-PRO-OH
    2. Synonyms: N-ALPHA-SUCCINYL-L-PROLINE;N-SUCCINYL-L-PROLINE;succinylproline;Succinyl-L-proline≥ 99% (TLC);Suc-L-Pro-OH;SUCCINYL-L-PROLINE;SUC-PROLINE;SUC-PRO-OH
    3. CAS NO:63250-32-8
    4. Molecular Formula: C9H13NO5
    5. Molecular Weight: 215.2
    6. EINECS: N/A
    7. Product Categories: A to;Angiotensin Converting Enzyme;Angiotensin Converting EnzymeEnzyme Inhibitors by Enzyme;Angiotensin Converting EnzymePeptides for Cell Biology;Enzyme Inhibitors;Protease Inhibitor Specificity Index;Protease Inhibitors
    8. Mol File: 63250-32-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 519.5°C at 760 mmHg
    3. Flash Point: 268°C
    4. Appearance: /
    5. Density: 1.425g/cm3
    6. Vapor Pressure: 3.46E-12mmHg at 25°C
    7. Refractive Index: 1.551
    8. Storage Temp.: −20°C
    9. Solubility: N/A
    10. PKA: 3.53±0.20(Predicted)
    11. CAS DataBase Reference: SUC-PRO-OH(CAS DataBase Reference)
    12. NIST Chemistry Reference: SUC-PRO-OH(63250-32-8)
    13. EPA Substance Registry System: SUC-PRO-OH(63250-32-8)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 63250-32-8(Hazardous Substances Data)

63250-32-8 Usage

Chemical Properties

White to off-white powder

Check Digit Verification of cas no

The CAS Registry Mumber 63250-32-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,2,5 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 63250-32:
(7*6)+(6*3)+(5*2)+(4*5)+(3*0)+(2*3)+(1*2)=98
98 % 10 = 8
So 63250-32-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H13NO5/c11-7(3-4-8(12)13)10-5-1-2-6(10)9(14)15/h6H,1-5H2,(H,12,13)(H,14,15)/t6-/m0/s1

63250-32-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Suc-Pro-OH

1.2 Other means of identification

Product number -
Other names SUC-PROLINE

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:63250-32-8 SDS

63250-32-8Downstream Products

63250-32-8Relevant articles and documents

Captopril analogues as metallo-β-lactamase inhibitors

Yusof, Yusralina,Tan, Daniel T.C.,Arjomandi, Omid Khalili,Schenk, Gerhard,McGeary, Ross P.

supporting information, p. 1589 - 1593 (2016/07/27)

A number of captopril analogues were synthesised and tested as inhibitors of the metallo-β-lactamase IMP-1. Structure–activity studies showed that the methyl group was unimportant for activity, and that the potencies of these inhibitors could be best improved by shortening the length of the mercaptoalkanoyl side-chain. Replacing the thiol group with a carboxylic acid led to complete loss of activity, and extending the length of the carboxylate group led to decreased potency. Good activity could be maintained by substituting the proline ring with pipecolic acid.

HYDROXYCARBAMOYLALKYLACYLPIPECOLIC ACID COMPOUNDS

-

, (2008/06/13)

New hydroxycarbamoylalkylacyl derivatives of pipecolic acid which have the general formula STR1 are useful as angiotensin converting enzyme inhibitors.

CARBOXYACYLPROLINE DERIVATIVES

-

, (2008/06/13)

New carboxyalkylacylamino acids which are derivatives of proline, pipecolic acid and azetidine-2-carboxylic acid and have the general formula STR1 are useful as angiotensin converting enzyme inhibitors.

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