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Ethyl 4-bromocyclohexanecarboxylate is a chemical compound with the molecular formula C9H15BrO2. It is an ester of bromocyclohexane and ethanol, known for its pleasant fruity odor. This colorless to pale yellow liquid is stable under normal temperature and pressure, but should be handled with care due to its potential harmful effects if inhaled, ingested, or causing skin and eye irritation.

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  • 190717-38-5 Structure
  • Basic information

    1. Product Name: ethyl 4-broMocyclohexanecarboxylate
    2. Synonyms: ethyl 4-broMocyclohexanecarboxylate
    3. CAS NO:190717-38-5
    4. Molecular Formula: C9H15BrO2
    5. Molecular Weight: 235.1182
    6. EINECS: -0
    7. Product Categories: N/A
    8. Mol File: 190717-38-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 88-89 °C(Press: 0.01 Torr)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.344±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: ethyl 4-broMocyclohexanecarboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 4-broMocyclohexanecarboxylate(190717-38-5)
    11. EPA Substance Registry System: ethyl 4-broMocyclohexanecarboxylate(190717-38-5)
  • 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: 190717-38-5(Hazardous Substances Data)

190717-38-5 Usage

Uses

Used in Flavoring Agents:
Ethyl 4-bromocyclohexanecarboxylate is used as a flavoring agent in the food and beverage industry, providing a pleasant fruity aroma to various products.
Used in Pharmaceutical Production:
Ethyl 4-bromocyclohexanecarboxylate serves as an intermediate in the production of pharmaceuticals, contributing to the synthesis of various medicinal compounds.
Used in Perfumery:
In the perfume industry, ethyl 4-bromocyclohexanecarboxylate is utilized as an intermediate for creating fragrances, capitalizing on its fruity scent to enhance the appeal of perfumes and other scented products.

Check Digit Verification of cas no

The CAS Registry Mumber 190717-38-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,7,1 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 190717-38:
(8*1)+(7*9)+(6*0)+(5*7)+(4*1)+(3*7)+(2*3)+(1*8)=145
145 % 10 = 5
So 190717-38-5 is a valid CAS Registry Number.

190717-38-5SDS

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 ethyl 4-bromocyclohexanecarboxylate

1.2 Other means of identification

Product number -
Other names ethyl 4-bromo cyclohexyl carboxylate

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:190717-38-5 SDS

190717-38-5Relevant articles and documents

METHOD FOR PURIFYING 4-HALO CYCLOHEXANE-1-CARBOXYLIC ACID, AND METHODS FOR PRODUCING PRODUCTS CONTAINING 4- HALO CYCLOHEXANE-1-CARBOXYLIC ACID

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Paragraph 0037-0038, (2020/03/31)

To provide a method for purifying a 4-halo cyclohexane-1-carboxylic acid which can be highly purified without performing column purification, and a method for producing a product containing the 4-halo cyclohexane-1-carboxylic acid.SOLUTION: There is provided a method for purifying a 4-halo cyclohexane-1-carboxylic acid comprising a crystallization step of subjecting a mixture including a 4-halo cyclohexane-1-carboxylic acid and a 3-halo cyclohexane-1-carboxylic acid to a crystallization operation in a mixed solvent of water and a water-soluble organic solvent or a hydrocarbon solvent to increase a content of the 4-halo cyclohexane-1-carboxylic acid.SELECTED DRAWING: None

Imidazole n-benzyldioxol derivatives, method for preparing same, resulting intermediates, pharmaceutical compositions and use of said derivatives as endothelin antagonists

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, (2008/06/13)

PCT No. PCT/FR96/01749 Sec. 371 Date Jun. 9, 1998 Sec. 102(e) Date Jun. 9, 1998 PCT Filed Nov. 7, 1996 PCT Pub. No. WO97/17339 PCT Pub. Date May 15, 1997The invention relates to the new products of formula (I): in which: R1 represents alkyl, optionally su

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