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475977-63-0

Carbamic acid, bromo-, 1,1-dimethylethyl 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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  • 475977-63-0 Structure

  • Basic information

    1. Product Name: Carbamic acid, bromo-, 1,1-dimethylethyl ester (9CI)
    2. Synonyms: Carbamic acid, bromo-, 1,1-dimethylethyl ester (9CI)
    3. CAS NO:475977-63-0
    4. Molecular Formula: C5H10BrNO2
    5. Molecular Weight: 196.0424
    6. EINECS: N/A
    7. Product Categories: N-BOC
    8. Mol File: 475977-63-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.435±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 5.84±0.46(Predicted)
    10. CAS DataBase Reference: Carbamic acid, bromo-, 1,1-dimethylethyl ester (9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: Carbamic acid, bromo-, 1,1-dimethylethyl ester (9CI)(475977-63-0)
    12. EPA Substance Registry System: Carbamic acid, bromo-, 1,1-dimethylethyl ester (9CI)(475977-63-0)

  • 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: 475977-63-0(Hazardous Substances Data)

475977-63-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 475977-63-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,5,9,7 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 475977-63:
(8*4)+(7*7)+(6*5)+(5*9)+(4*7)+(3*7)+(2*6)+(1*3)=220
220 % 10 = 0
So 475977-63-0 is a valid CAS Registry Number.

475977-63-0Upstream product

475977-63-0Downstream Products

475977-63-0Relevant articles and documents

t-Butyl N,N-dibromocarbamate (BBC) - New reagent for aminobromination of terminal alkenes

Klepacz, Anna,Zwierzak, Andrzej

, p. 4539 - 4540 (2007/10/03)

t-Butyl N,N-dibromocarbamate, easily obtained by bromination of t-butyl carbamate in aqueous potassium carbonate, reacts smoothly with a variety of terminal alkenes to afford the corresponding β-bromo-N-Boc-amines upon reduction with aqueous sodium sulphi

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