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CAS

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82912-90-1

5-Chloro-6,6-dimethyl-2,5,6,7-tetrahydro-[2]pyrindin-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 82912-90-1 Structure

  • Basic information

    1. Product Name: 5-Chloro-6,6-dimethyl-2,5,6,7-tetrahydro-[2]pyrindin-1-one
    2. Synonyms:
    3. CAS NO:82912-90-1
    4. Molecular Formula:
    5. Molecular Weight: 197.664
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 82912-90-1.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: 5-Chloro-6,6-dimethyl-2,5,6,7-tetrahydro-[2]pyrindin-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-Chloro-6,6-dimethyl-2,5,6,7-tetrahydro-[2]pyrindin-1-one(82912-90-1)
    11. EPA Substance Registry System: 5-Chloro-6,6-dimethyl-2,5,6,7-tetrahydro-[2]pyrindin-1-one(82912-90-1)

  • 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: 82912-90-1(Hazardous Substances Data)

82912-90-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82912-90-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,9,1 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 82912-90:
(7*8)+(6*2)+(5*9)+(4*1)+(3*2)+(2*9)+(1*0)=141
141 % 10 = 1
So 82912-90-1 is a valid CAS Registry Number.

82912-90-1Downstream Products

82912-90-1Relevant articles and documents

A NOVEL PHOTOCHEMICAL PRENYLATION REACTION OF HETEROAROMATICS INVOLVING AN ENONE FUNCTION IN THEIR RING SYSTEM

Naito, Toshihiko,Momose, Yu,Kaneko, Chikara

, p. 1531 - 1534 (2007/10/02)

In a novel photochemical prenylation of heteroaromatics involving an enone function in their ring system, the key step is an acid-catalyzed C-C bond fission in the head-to-tail adduct formed by photocycloaddition of these heteroaromatics to 2-methyl-3-buten-2-ol to give the heteroaromatics having a 3-methylbut-2-enyl function (or its equivalent) at the α-position of the enone system.Examples using 2-quinolones, 2-pyridones, and coumarins are reported.KEYWORDS---photochemical synthesis; photochemical prenylation; 3,3-dimethylallyalation of heteroaromatics; photochemical 2+2 cycloaddition; 3-(3-methylbut-2-enyl)-2-quinolones; 2-methyl-3-buten-2-ol as prenylation reagent; synthesis of khaplofoline

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