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1541-17-9

Carbamic acid, 3-cyclohexen-1-yl-, ethyl ester is a chemical compound with the molecular formula C9H15NO2. It is an ester derivative of carbamic acid, featuring a cyclohexenyl group attached to the carbamic acid moiety. Carbamic acid, 3-cyclohexen-1-yl-, ethyl ester is characterized by its unique structure, which includes a cyclohexene ring with a double bond at the 3-position and an ethyl ester group. It is an organic compound that may be used in various chemical reactions and synthesis processes, particularly in the pharmaceutical and agrochemical industries. Due to its specific functional groups and structural features, it can participate in a range of chemical transformations, making it a potentially valuable intermediate in the synthesis of more complex molecules.

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  • 1541-17-9 Structure

  • Basic information

    1. Product Name: Carbamic acid, 3-cyclohexen-1-yl-, ethyl ester
    2. Synonyms:
    3. CAS NO:1541-17-9
    4. Molecular Formula: C9H15NO2
    5. Molecular Weight: 169.224
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1541-17-9.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: Carbamic acid, 3-cyclohexen-1-yl-, ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Carbamic acid, 3-cyclohexen-1-yl-, ethyl ester(1541-17-9)
    11. EPA Substance Registry System: Carbamic acid, 3-cyclohexen-1-yl-, ethyl ester(1541-17-9)

  • 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: 1541-17-9(Hazardous Substances Data)

1541-17-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1541-17-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,4 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1541-17:
(6*1)+(5*5)+(4*4)+(3*1)+(2*1)+(1*7)=59
59 % 10 = 9
So 1541-17-9 is a valid CAS Registry Number.

1541-17-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl N-(cyclohex-3-en-1-yl)carbamate

1.2 Other means of identification

Product number -
Other names Ethyl-N-(4-cyclohexenyl)-carbamat

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:1541-17-9 SDS

1541-17-9Downstream Products

1541-17-9Relevant articles and documents

Synthesis and transformations of alkyl N-(1-cyclohex-3-enyl)carbamates prepared from cyclohex-3-ene carboxylic acid via Curtius rearrangement

Gómez-Sánchez, Elena,Marco-Contelles, José

, p. 1207 - 1219 (2007/10/03)

The Curtius rearrangement of cyclohex-3-ene carboxylic acid using diphenylphosphoryl azide in the presence of triethylamime and ethanol, t-butanol or benzyl alcohol has been described. As a result the synthesis of ethyl, t-butyl or benzyl N-(1-cyclohex-3-enyl)carbamates has been achieved in one pot, in good chemical yield. A series of transformations of benzyl N-(1-cyclohex-3-enyl)carbamate, such as iodination and epoxidation, as well as opening of the corresponding ring epoxide, have been carried out leading to some useful oxygenated cyclohexylamimo building blocks.

CAN (ETHOXYCARBONYL)NITRENE SELECTIVITY BE CONTROLLED BY MICELLAR PSEUDOPHASE?

Bertolaccini, Riccardo,Cerichelli, Giorgio,Loreto, M. Antonietta,Pellacani, Lucio,Tardella, Paolo A.

, p. 587 - 588 (2007/10/02)

The effect of cationic surfactants in the reaction of cyclohexene and (ethoxycarbonyl)nitrene has been studied.When the counter-ion of the surfactant was bromide, the products of bromination of cyclohexene or those requiring the intermediacy of nitrene were observed.The latter were the only products if nitrate was the counter-ion of the surfactant, using N-oxy>urethan, even without added base.

Solvolytic Rearrangements of Azabicyclic Compounds. Part 1. Identification of Products

Bastable, John W.,Cooper, Anthony J.,Dunkin, Ian R.,Hobson, John D.,Riddell, William D.

, p. 1339 - 1345 (2007/10/02)

The products of solvolysis of 2β-hylogeno-derivatives of 7-methyl-7-azabicycloheptane, 8-methyl-8-azabicyclooctane, 9-methyl-9-azabicyclo-- and --nonane, and 7-methyl-7-azabicyclooctane, have been isolated and characteri

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