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172299-70-6

3-Cyclohexene-1-carboxylic acid, 1-(acetylamino)-, methyl ester (9CI) is a chemical compound with the molecular formula C12H17NO3. It is a methyl ester derivative of 3-cyclohexene-1-carboxylic acid, which is a carboxylic acid compound with a cyclohexene ring. 3-Cyclohexene-1-carboxylicacid,1-(acetylamino)-,methylester(9CI) contains an acetylamino group, which is a functional group containing an amide bonded to an acetyl group. It is commonly used in organic synthesis and pharmaceutical research due to its potential pharmacological and biological activities.

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  • 172299-70-6 Structure

  • Basic information

    1. Product Name: 3-Cyclohexene-1-carboxylicacid,1-(acetylamino)-,methylester(9CI)
    2. Synonyms: 3-Cyclohexene-1-carboxylicacid,1-(acetylamino)-,methylester(9CI);methyl 1-acetamidocyclohex-3-enecarboxylate;Methyl 1-acetamido-3-cyclohexene-1-carboxylate
    3. CAS NO:172299-70-6
    4. Molecular Formula: C10H15NO3
    5. Molecular Weight: 197.24
    6. EINECS: N/A
    7. Product Categories: AMINOACID
    8. Mol File: 172299-70-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-Cyclohexene-1-carboxylicacid,1-(acetylamino)-,methylester(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Cyclohexene-1-carboxylicacid,1-(acetylamino)-,methylester(9CI)(172299-70-6)
    11. EPA Substance Registry System: 3-Cyclohexene-1-carboxylicacid,1-(acetylamino)-,methylester(9CI)(172299-70-6)

  • 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: 172299-70-6(Hazardous Substances Data)

172299-70-6 Usage

Uses

Used in Organic Synthesis:
3-Cyclohexene-1-carboxylic acid, 1-(acetylamino)-, methyl ester (9CI) is used as a building block for the synthesis of other organic compounds. Its unique structure and functional groups make it a valuable intermediate in the preparation of various organic molecules.
Used in Pharmaceutical Research:
3-Cyclohexene-1-carboxylic acid, 1-(acetylamino)-, methyl ester (9CI) is used as a starting material in the development of new drugs. Its potential pharmacological and biological activities make it a promising candidate for the discovery of novel therapeutic agents.
Used in Chemistry and Biochemistry:
3-Cyclohexene-1-carboxylic acid, 1-(acetylamino)-, methyl ester (9CI) is used in various chemical and biochemical applications. Its unique structure and functional groups allow for its use in the study of chemical reactions and biological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 172299-70-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,2,9 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 172299-70:
(8*1)+(7*7)+(6*2)+(5*2)+(4*9)+(3*9)+(2*7)+(1*0)=156
156 % 10 = 6
So 172299-70-6 is a valid CAS Registry Number.

172299-70-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Cyclohexene-1-carboxylicacid,1-(acetylamino)-,methylester(9CI)

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

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More Details:172299-70-6 SDS

172299-70-6Relevant articles and documents

Regioselective ring-opening metathesis - Cross metathesis of bridgehead-substituted 7-azanprbornene

Carreras,Avenoza,Busto,Peregrina

, p. 1235 - 1238 (2007)

Figure presented In this paper we describe a highly regioselective ring-opening metathesis-cross metathesis (ROM-CM) process between methyl N-Boc-7-azabicyclo[2.2.1]hept-2-en-1-carboxylate, a bridgehead-substituted 7-azanorbornene system, and electron-poo

Peptide-based short single β-strand mimics without hydrogen bonding or aggregation

Zhai, Luhan,Otani, Yuko,Hori, Yukiko,Tomita, Taisuke,Ohwada, Tomohiko

, p. 1573 - 1576 (2020)

Generation of short peptides with a single β-strand structure in solution is difficult. Herein, we design a new class of single β-strand peptidic mimics that are stable without self-aggregation in protic and non-protic solvents. Introduction of one presen

Unexpectedly rigid short peptide foldamers in which NH-π and CH-π interactions are preserved in solution

Nara, Masayuki,Ohwada, Tomohiko,Otani, Yuko,Zhai, Luhan

supporting information, p. 8344 - 8347 (2021/08/25)

NH-π and CH-π interactions, due to their weak character, are not easily identified in solution. We report a group of isolable short peptides with stable folds, in which NH-π and CH-π main chain-side chain interactions can be detected in solution by means

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