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4-Piperidinecarboxylic acid, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 103824-89-1 Structure
  • Basic information

    1. Product Name: 4-Piperidinecarboxylic acid, phenylmethyl ester
    2. Synonyms:
    3. CAS NO:103824-89-1
    4. Molecular Formula: C13H17NO2
    5. Molecular Weight: 219.283
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 103824-89-1.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: 4-Piperidinecarboxylic acid, phenylmethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Piperidinecarboxylic acid, phenylmethyl ester(103824-89-1)
    11. EPA Substance Registry System: 4-Piperidinecarboxylic acid, phenylmethyl ester(103824-89-1)
  • 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: 103824-89-1(Hazardous Substances Data)

103824-89-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103824-89-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,8,2 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 103824-89:
(8*1)+(7*0)+(6*3)+(5*8)+(4*2)+(3*4)+(2*8)+(1*9)=111
111 % 10 = 1
So 103824-89-1 is a valid CAS Registry Number.

103824-89-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl piperidine-4-carboxylate

1.2 Other means of identification

Product number -
Other names 4-Piperidinecarboxylic acid,phenylmethyl ester

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:103824-89-1 SDS

103824-89-1Relevant articles and documents

INHIBITORS OF (ALPHA-V)(BETA-6) INTEGRIN

-

Paragraph 0424; 0425, (2018/09/16)

Disclosed are small molecule inhibitors of αvβ6 integrin, and methods of using them to treat a number of diseases and conditions.

Design and synthesis of new peptidomimetics as potential inhibitors of MurE

Zivec, Matej,Turk, Samo,Blanot, Didier,Gobec, Stanislav

experimental part, p. 95 - 109 (2012/05/04)

With the continuing emergence and spread of multidrug-resistant bacteria, there is an urgent need for the development of new antimicrobial agents. One possible source of new antibacterial targets is the biosynthesis of the bacterial cellwall peptidoglycan

PYRAZOLONE COMPOUNDS AS METABOTROPIC GLUTAMATE RECEPTOR AGONISTS FOR THE TREATMENT OF NEUROLOGICAL AND PSYCHIATRIC DISORDERS

-

Page/Page column 254; 255, (2008/06/13)

Compounds of Formula (I), wherein R1, R2, R3, R4, R5, R6, X, and n are as defined for Formula (I) in the description, processes for the preparation of the compounds and new intermediates employed in the preparation, pharmaceutical compositions containing the compounds, and the use of the compounds in the treatment or prevention of neurological and psychiatric disorders associated with glutamate dysfunction.

Prenyl carbamates: Preparation and deprotection

Vatèle, Jean-Michel

, p. 4251 - 4260 (2007/10/03)

Prenyloxycarbonylimidazole (PreocIm) and prenyl p-nitrophenyl carbonate (PreocOC6H4p-NO2), two substitutes for the unstable prenyl chloroformate, allowed an efficient introduction of the prenyloxycarbonyl group to a variety of primary and secondary amines. Deprotection of prenyl carbamates was readily achieved by, first their conversion to 2-iodo-3-methoxy-3-methylbutyl carbamates with iodine in methanol followed by reductive β-elimination with zinc powder. These reaction conditions are compatible with the presence of a number of functional groups such as Boc and Cbz carbamates, sulfides, double bonds, indoles and aromatic ethers.

One-pot selective cleavage of prenyl carbamates using iodine in methanol followed by zinc

Vatele, Jean-Michel

, p. 9127 - 9130 (2007/10/03)

The prenyloxycarbonyl (Preoc) moiety was efficiently removed from carbamates to provde the corresponding amines in good to excellent yields (63-88 percent) by using iodine in methanol followed by treatment of the resulting β-methoxyiodides by zinc powder. The reaction conditions are compatible with the presence of a number of functional groups such as Boc and Cbz carbamates, sulfides, double bonds, indoles and aromatic methyl ethers.

Naphthrydine compounds and their azaisosteric analogues as antibacterials

-

, (2008/06/13)

Piperidine derivatives of formula (I) or a pharmaceutically acceptable derivative thereof and pharmaceutically acceptable derivatives thereof useful in methods of treatment of bacterial infections in mammals, particularly in man.

QUINOLINE DERIVATIVES AND THEIR USE AS ANTIBACTERIAL AGENTS

-

Page/Page column 11, (2010/11/30)

Aminopiperidine derivatives and pharmaceutically acceptable derivatives thereof useful in methods of treatment of bacterial infections in mammals, particularly in man.

Spirocyclic nonpeptide glycoprotein IIb-IIIa antagonists. Part 1: Design of potent and specific 3,9-diazaspiro[5.5]undecanes

Smyth,Rose,Mehrotra,Heath,Ruhter,Schotten,Seroogy,Volkots,Pandey,Scarborough

, p. 1289 - 1292 (2007/10/03)

The synthesis and biological activity of novel glycoprotein IIb-IIIa antagonists containing the 3,9-diazaspiro[5.5]undecane nucleus are described. The potent activity of these compounds as platelet aggregation inhibitors demonstrates the utility of the spirocyclic structures as a central template for nonpeptide RGD mimics.

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