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(3aS,4S,5S,6R,7aS)-4-(ethoxycarbonyl)-6-ethyl-1-oxooctahydro-1H-indene-5-carboxylic acid is a carboxylic acid compound with a molecular formula of C15H22O4 and a molecular weight of 266.33 g/mol. It features a carbonyl group, an ethyl group, and a carboxylic acid group, making it a significant intermediate in organic synthesis.

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  • (3aS,4S,5S,6R,7aS)-4-(ethoxycarbonyl)-6-ethyl-1-oxooctahydro-1H-indene-5-carboxylic acid

    Cas No: 130274-13-4

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  • 130274-13-4 Structure
  • Basic information

    1. Product Name: (3aS,4S,5S,6R,7aS)-4-(ethoxycarbonyl)-6-ethyl-1-oxooctahydro-1H-indene-5-carboxylic acid
    2. Synonyms: (3aS,4S,5S,6R,7aS)-4-(ethoxycarbonyl)-6-ethyl-1-oxooctahydro-1H-indene-5-carboxylic acid
    3. CAS NO:130274-13-4
    4. Molecular Formula: C15H22O5
    5. Molecular Weight: 282.33218
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 130274-13-4.mol
  • Chemical Properties

    1. Melting Point: 151-152 °C
    2. Boiling Point: 431.8±45.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.170±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 4.23±0.60(Predicted)
    10. CAS DataBase Reference: (3aS,4S,5S,6R,7aS)-4-(ethoxycarbonyl)-6-ethyl-1-oxooctahydro-1H-indene-5-carboxylic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: (3aS,4S,5S,6R,7aS)-4-(ethoxycarbonyl)-6-ethyl-1-oxooctahydro-1H-indene-5-carboxylic acid(130274-13-4)
    12. EPA Substance Registry System: (3aS,4S,5S,6R,7aS)-4-(ethoxycarbonyl)-6-ethyl-1-oxooctahydro-1H-indene-5-carboxylic acid(130274-13-4)
  • 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: 130274-13-4(Hazardous Substances Data)

130274-13-4 Usage

Uses

Used in Pharmaceutical Industry:
(3aS,4S,5S,6R,7aS)-4-(ethoxycarbonyl)-6-ethyl-1-oxooctahydro-1H-indene-5-carboxylic acid is used as a key intermediate in the synthesis of various pharmaceutical compounds due to its unique structure and reactivity.
Used in Agrochemical Industry:
(3aS,4S,5S,6R,7aS)-4-(ethoxycarbonyl)-6-ethyl-1-oxooctahydro-1H-indene-5-carboxylic acid is also utilized as an intermediate in the development of agrochemicals, contributing to the creation of effective products for agricultural applications.
Used in Organic Synthesis:
(3aS,4S,5S,6R,7aS)-4-(ethoxycarbonyl)-6-ethyl-1-oxooctahydro-1H-indene-5-carboxylic acid serves as a valuable building block in organic synthesis, enabling the production of a wide range of chemical products.
Further research and experimentation may reveal additional properties and potential uses for this versatile compound in various industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 130274-13-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,2,7 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 130274-13:
(8*1)+(7*3)+(6*0)+(5*2)+(4*7)+(3*4)+(2*1)+(1*3)=84
84 % 10 = 4
So 130274-13-4 is a valid CAS Registry Number.

130274-13-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (3aS,4S,5S,6R,7aS)-4-(Ethoxycarbonyl)-6-ethyl-1-oxooctahydro-1H-i ndene-5-carboxylic 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:130274-13-4 SDS

130274-13-4Relevant articles and documents

The Synthesis of (+/-)-Coronafacic Acid by a Tandem Wessely Oxidation-Diels-Alder Reaction Sequence

Bhamare, N. K.,Granger, Thierry,Macas, T. S.,Yates, Peter

, p. 739 - 740 (2007/10/02)

(+/-)-Coronafacic acid (9) has been synthesized from ethyl 5-(4-ethyl-2-hydroxyphenyl)pent-2-enoate (4) via a tandem Wessely oxidation-Diels-Alder reaction sequence.

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