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CAS

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166271-53-0

Carbamic acid, (3-hydroxy-1,1-dimethylbutyl)-, methyl ester (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 166271-53-0 Structure

  • Basic information

    1. Product Name: Carbamic acid, (3-hydroxy-1,1-dimethylbutyl)-, methyl ester (9CI)
    2. Synonyms: Carbamic acid, (3-hydroxy-1,1-dimethylbutyl)-, methyl ester (9CI)
    3. CAS NO:166271-53-0
    4. Molecular Formula: C8H17NO3
    5. Molecular Weight: 175.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 166271-53-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Carbamic acid, (3-hydroxy-1,1-dimethylbutyl)-, methyl ester (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Carbamic acid, (3-hydroxy-1,1-dimethylbutyl)-, methyl ester (9CI)(166271-53-0)
    11. EPA Substance Registry System: Carbamic acid, (3-hydroxy-1,1-dimethylbutyl)-, methyl ester (9CI)(166271-53-0)

  • 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: 166271-53-0(Hazardous Substances Data)

166271-53-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 166271-53-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,2,7 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 166271-53:
(8*1)+(7*6)+(6*6)+(5*2)+(4*7)+(3*1)+(2*5)+(1*3)=140
140 % 10 = 0
So 166271-53-0 is a valid CAS Registry Number.

166271-53-0Relevant articles and documents

Interaction of methyl N-(3-oxoalkyl)carbamates, S-methyl-carbamates, and -dithiocarbamates with sodium borohydride. Synthesis of tetrahydro-1,3-oxazin-2-ones and -thiones

Fisyuk,Ryzhova,Unkovskii

, p. 597 - 609 (2007/10/03)

The interaction of N-(3-oxoalkyl)carbamates, -thiocarbamates, and -dithiocarbamates with sodium borohydride has been studied. It was shown that reaction proceeds diastereoselectively, and reductive cyclization with the formation of tetrahydro-1,3-oxazin-2-ones and -thiones may occur. The tend to cyclization of the N-(3-hydroxyalkyl)carbamates, -thiocarbamates, and -dithiocarbamates formed as intermediates depends on the number of substituents in the alkyl chain.

SYNTHESIS OF TETRAHYDRO-1,3-OXAZIN-2-ONES AND -2-THIONES FROM ESTERS OF N-(3-OXOALKYL)CARBAMIC AND -DITHIOCARBAMIC ACIDS

Fisyuk, A. S.,Ryzhova, E. V.,Unkovskii, B. V.

, p. 238 - 242 (2007/10/02)

A study has been made of the interaction of N-(3-oxoalkyl)carbamates and -dithiocarbamates with sodium borohydride; it has been shown that, depending on the pH of the reaction medium, the interaction may produce either tetrahydro-1,3-oxazin-2-ones and -2-

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