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3-hydroxy-5-methyl-3-(2-oxocyclohexyl)indolin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 85778-05-8 Structure
  • Basic information

    1. Product Name: 3-hydroxy-5-methyl-3-(2-oxocyclohexyl)indolin-2-one
    2. Synonyms:
    3. CAS NO:85778-05-8
    4. Molecular Formula:
    5. Molecular Weight: 259.305
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 85778-05-8.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: 3-hydroxy-5-methyl-3-(2-oxocyclohexyl)indolin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-hydroxy-5-methyl-3-(2-oxocyclohexyl)indolin-2-one(85778-05-8)
    11. EPA Substance Registry System: 3-hydroxy-5-methyl-3-(2-oxocyclohexyl)indolin-2-one(85778-05-8)
  • 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: 85778-05-8(Hazardous Substances Data)

85778-05-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85778-05-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,7,7 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 85778-05:
(7*8)+(6*5)+(5*7)+(4*7)+(3*8)+(2*0)+(1*5)=178
178 % 10 = 8
So 85778-05-8 is a valid CAS Registry Number.

85778-05-8Downstream Products

85778-05-8Relevant articles and documents

In situ formed bifunctional primary amine-imine catalyst: Application to the construction of chiral tertiary alcohols through asymmetric aldol-type reaction

Mao, Zhijie,Zhu, Xi,Lin, Aijun,Li, Weipeng,Shi, Yan,Mao, Haibin,Zhu, Chengjian,Cheng, Yixiang

, p. 2029 - 2036 (2013)

An in situ formation method to obtain chiral bifunctional primary amine-imine catalysts from the C2-symmetric chiral diimines has been developed. The efficiency of this method in the construction of chiral tertiary alcohols which are valuable p

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