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CAS

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173898-21-0

Benzamide, 4-(1-aminoethyl)-, (R)is a chemical compound belonging to the Benzenoids class of organic compounds. It is characterized by a benzene ring, a benzamide functional group, and a specific chiral center denoted as (R), which indicates the direction of the molecule's rotation of plane-polarized light. With a molecular formula of C9H12N2O, this compound is utilized in the synthesis of other organic compounds and for scientific research purposes. Due to its potential toxicity and reactivity, it is crucial to handle this compound with appropriate safety measures.

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  • 173898-21-0 Structure

  • Basic information

    1. Product Name: Benzamide, 4-(1-aminoethyl)-, (R)-
    2. Synonyms: Benzamide, 4-(1-aminoethyl)-, (R)-;Benzamide, 4-(1-aminoethyl)-, (R)- (9CI);(R)-4-(1-AMinoethyl)benzaMide;4-[(1R)-1-aminoethyl]benzamide
    3. CAS NO:173898-21-0
    4. Molecular Formula: C9H12N2O
    5. Molecular Weight: 164.21
    6. EINECS: N/A
    7. Product Categories: API intermediates
    8. Mol File: 173898-21-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 326.759 °C at 760 mmHg
    3. Flash Point: 151.419 °C
    4. Appearance: /
    5. Density: 1.129 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. PKA: 16.20±0.50(Predicted)
    10. CAS DataBase Reference: Benzamide, 4-(1-aminoethyl)-, (R)-(CAS DataBase Reference)
    11. NIST Chemistry Reference: Benzamide, 4-(1-aminoethyl)-, (R)-(173898-21-0)
    12. EPA Substance Registry System: Benzamide, 4-(1-aminoethyl)-, (R)-(173898-21-0)

  • 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: 173898-21-0(Hazardous Substances Data)

173898-21-0 Usage

Uses

Used in Organic Synthesis:
Benzamide, 4-(1-aminoethyl)-, (R)is used as a building block for the synthesis of various organic compounds, contributing to the development of new chemical entities with potential applications in different industries.
Used in Scientific Research:
Benzamide, 4-(1-aminoethyl)-, (R)serves as a valuable research tool in the field of chemistry, particularly in studies focused on the properties and behavior of chiral molecules and their interactions with other substances. It aids in understanding the fundamental principles of stereochemistry and its implications in chemical reactions and molecular structures.

Check Digit Verification of cas no

The CAS Registry Mumber 173898-21-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,8,9 and 8 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 173898-21:
(8*1)+(7*7)+(6*3)+(5*8)+(4*9)+(3*8)+(2*2)+(1*1)=180
180 % 10 = 0
So 173898-21-0 is a valid CAS Registry Number.

173898-21-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(1R)-1-aminoethyl]benzamide

1.2 Other means of identification

Product number -
Other names Benzamide,4-(1-aminoethyl)-,(R)

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:173898-21-0 SDS

173898-21-0Downstream Products

173898-21-0Relevant articles and documents

NOVEL HETEROCYCLIC COMPOUNDS AS INHIBITORS OF VANIN-1 ENZYME

-

Page/Page column 110; 111, (2016/12/22)

Compounds, pharmaceutically acceptable salts thereof, are disclosed wherein the compounds have the structure of Formula (I) as defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.

Novel peptoid building blocks: Synthesis of functionalized aromatic helix-inducing submonomers

Seo, Jiwon,Barron, Annelise E.,Zuckermann, Ronald N.

supporting information; experimental part, p. 492 - 495 (2010/05/02)

[Chemical equation presented] Peptoids, oligo-N-substituted glycines, can fold into well-defined helical secondary structures. The design and synthesis of new peptoid building blocks that are capable of both (a) inducing a helical secondary structure and

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