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2,7-Octadien-1-ol, 6-chloro-3,7-dimethyl-, acetate, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 74514-19-5 Structure
  • Basic information

    1. Product Name: 2,7-Octadien-1-ol, 6-chloro-3,7-dimethyl-, acetate, (E)-
    2. Synonyms:
    3. CAS NO:74514-19-5
    4. Molecular Formula: C12H19ClO2
    5. Molecular Weight: 230.735
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 74514-19-5.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: 2,7-Octadien-1-ol, 6-chloro-3,7-dimethyl-, acetate, (E)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,7-Octadien-1-ol, 6-chloro-3,7-dimethyl-, acetate, (E)-(74514-19-5)
    11. EPA Substance Registry System: 2,7-Octadien-1-ol, 6-chloro-3,7-dimethyl-, acetate, (E)-(74514-19-5)
  • 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: 74514-19-5(Hazardous Substances Data)

74514-19-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74514-19-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,5,1 and 4 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 74514-19:
(7*7)+(6*4)+(5*5)+(4*1)+(3*4)+(2*1)+(1*9)=125
125 % 10 = 5
So 74514-19-5 is a valid CAS Registry Number.

74514-19-5Relevant articles and documents

Rapid Oxidation Indoles into 2-Oxindoles Mediated by PIFA in Combination with n-Bu4NCl ? H2O

Liang, Peng,Zhao, Hang,Zhou, Tingting,Zeng, Kaiyun,Jiao, Wei,Pan, Yang,Liu, Yazhou,Fang, Dongmei,Ma, Xiaofeng,Shao, Huawu

, p. 3532 - 3538 (2021)

We report the development of a rapid approach for directly converting indoles into 2-oxindoles promoted by HOCl formed in situ from the combination of (bis(trifluoroacetoxy) iodo)benzene (PIFA) and n-Bu4NCl ? H2O. The procedure is widely functional group tolerant and provides 2-oxindoles in up to 95% yield within 5 min. The potential applications of the developed methodology are demonstrated by the gram-scale preparation of 3-methyl-2-oxindole (11 a), the one-pot two-step syntheses of spiro-oxindoles 26 a and 26 b, and the formal synthesis of (-)-folicanthine (2). (Figure presented.).

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