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CAS

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60705-21-7

2-Cyclohexene-1-carboxylic acid, 2-formyl-1,3-dimethyl-4-oxo-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 60705-21-7 Structure

  • Basic information

    1. Product Name: 2-Cyclohexene-1-carboxylic acid, 2-formyl-1,3-dimethyl-4-oxo-, methyl ester
    2. Synonyms:
    3. CAS NO:60705-21-7
    4. Molecular Formula: C11H14O4
    5. Molecular Weight: 210.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 60705-21-7.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: 2-Cyclohexene-1-carboxylic acid, 2-formyl-1,3-dimethyl-4-oxo-, methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Cyclohexene-1-carboxylic acid, 2-formyl-1,3-dimethyl-4-oxo-, methyl ester(60705-21-7)
    11. EPA Substance Registry System: 2-Cyclohexene-1-carboxylic acid, 2-formyl-1,3-dimethyl-4-oxo-, methyl ester(60705-21-7)

  • 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: 60705-21-7(Hazardous Substances Data)

60705-21-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60705-21-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,7,0 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 60705-21:
(7*6)+(6*0)+(5*7)+(4*0)+(3*5)+(2*2)+(1*1)=97
97 % 10 = 7
So 60705-21-7 is a valid CAS Registry Number.

60705-21-7SDS

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 Methyl 1,3-Dimethyl-2-formyl-4-oxocyclohex-2-enyl-1-carboxylat

1.2 Other means of identification

Product number -
Other names 2-Formyl-1,3-dimethyl-4-oxo-cyclohex-2-enecarboxylic acid methyl ester

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:60705-21-7 SDS

60705-21-7Downstream Products

60705-21-7Relevant articles and documents

Detours en route to a total synthesis of (+)-cassiol

Colombo, Maria I.,Zinczuk, Juan,Bohn, Maria L.,Ruveda, Edmundo A.

, p. 717 - 725 (2007/10/03)

A synthesis of the antiulcerogenic compound (+)-cassiol 1b has been achieved in 43% yield starting with lactol (S)-2 and sulfone 26. This short and efficient synthesis features the one-pot Julia olefination reaction of the sodium anion of (S)-2 with 26, through the key intermediate (-)-9. This synthesis has been developed as a result of exploratory experiments including different olefination reactions on 2. An attempt to synthesize the intermediate 9 by an intramolecular aldol condensation approach of the open chain precursor 4 is also described.

Stereoselective Synthesis of Trisporic Acids A and B, Their Methyl Esters, and Trisporols A and B, Hormones and Prohormones of Mucoraceous Fungi

White, James D.,Takabe, Kunihiko,Prisbylla, Michael P.

, p. 5233 - 5244 (2007/10/02)

Syntheses of (9E)- and (9Z)-trisporic acids A (1 and 4) and B (2 and 5) and the corresponding methyl esters (7, 10, 8, and 11, respectively) were accomplished via the Wittig reaction of lactol 52 with an appropriate phosphorane.The lactol was prepared by

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