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CAS

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435270-83-0

3-(4-BENZYL-PIPERIDIN-1-YL)-PROPIONIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 435270-83-0 Structure

  • Basic information

    1. Product Name: 3-(4-BENZYL-PIPERIDIN-1-YL)-PROPIONIC ACID
    2. Synonyms: TIMTEC-BB SBB011898;3-(4-BENZYL-PIPERIDIN-1-YL)-PROPIONIC ACID
    3. CAS NO:435270-83-0
    4. Molecular Formula: C15H21NO2
    5. Molecular Weight: 247.33
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 435270-83-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 401.4±28.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.101±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 3.83±0.10(Predicted)
    10. CAS DataBase Reference: 3-(4-BENZYL-PIPERIDIN-1-YL)-PROPIONIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-(4-BENZYL-PIPERIDIN-1-YL)-PROPIONIC ACID(435270-83-0)
    12. EPA Substance Registry System: 3-(4-BENZYL-PIPERIDIN-1-YL)-PROPIONIC ACID(435270-83-0)

  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 435270-83-0(Hazardous Substances Data)

435270-83-0 Usage

Common abbreviation

BPPA

Chemical structure

Consists of a piperidine ring with a benzyl group and a propionic acid moiety

Use

Synthetic intermediate in the production of pharmaceuticals and agrochemicals

Biological activities

Selective dopamine D1 receptor partial agonist, potential candidate for the treatment of neurological disorders such as Parkinson's disease, potential as an analgesic and anti-inflammatory agent

Unique properties

Unique structure and diverse pharmacological properties

Value

Valuable compound for research and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 435270-83-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,5,2,7 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 435270-83:
(8*4)+(7*3)+(6*5)+(5*2)+(4*7)+(3*0)+(2*8)+(1*3)=140
140 % 10 = 0
So 435270-83-0 is a valid CAS Registry Number.

435270-83-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-Benzyl-piperidin-1-yl)-propionic acid

1.2 Other means of identification

Product number -
Other names -

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:435270-83-0 SDS

435270-83-0Relevant articles and documents

Design and synthesis of some new carboxamide and propanamide derivatives bearing phenylpyridazine as a core ring and the investigation of their inhibitory potential on in-vitro acetylcholinesterase and butyrylcholinesterase

Kilic, Burcu,Gulcan, Hayrettin O.,Aksakal, Fatma,Ercetin, Tugba,Oruklu, Nihan,Umit Bagriacik,Dogruer, Deniz S.

, p. 235 - 249 (2018/05/24)

A series of new carboxamide and propanamide derivatives bearing phenylpyridazine as a core ring were designed, synthesized and evaluated for their ability to inhibit both cholinesterase enzymes. In addition, a series of carboxamide and propanamide derivat

Nitrogen-based camptothecin derivatives

-

, (2008/06/13)

(20S) esters of camptothecin analogs are provided. The compounds are (20S) esters of an aminoalkanoic acid or an imidoalkanoic acid and camptothecin, which is optionally substituted at the 7, 9, 10, 11, and 12 positions of the camptothecin ring. The compounds are useful for treating cancer.

NITROGEN-BASED HOMO-CAMPTOTHECIN DERIVATIVES

-

Page 53-55, (2008/06/13)

(20) esters of camptothecin analogs are provided. The compounds are (20) esters of an aminoalkanoic acid or an imidoalkanoic acid and homocamptothecin, which is optionally substituted at the 7, 9, 10, 11, and 12 positions of the homocamptothecin ring. The

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