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104478-98-0

methyl N-(4-amino-2-methoxyphenyl)carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 104478-98-0 Structure

  • Basic information

    1. Product Name: methyl N-(4-amino-2-methoxyphenyl)carbamate
    2. Synonyms: methyl N-(4-amino-2-methoxyphenyl)carbamate
    3. CAS NO:104478-98-0
    4. Molecular Formula: C9H12N2O3
    5. Molecular Weight: 196.20318
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 104478-98-0.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: methyl N-(4-amino-2-methoxyphenyl)carbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl N-(4-amino-2-methoxyphenyl)carbamate(104478-98-0)
    11. EPA Substance Registry System: methyl N-(4-amino-2-methoxyphenyl)carbamate(104478-98-0)

  • 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: 104478-98-0(Hazardous Substances Data)

104478-98-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104478-98-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,4,7 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 104478-98:
(8*1)+(7*0)+(6*4)+(5*4)+(4*7)+(3*8)+(2*9)+(1*8)=130
130 % 10 = 0
So 104478-98-0 is a valid CAS Registry Number.

104478-98-0Downstream Products

104478-98-0Relevant articles and documents

SUBSTITUTED P-DIAMINOBENZENE DERIVATIVES

-

Page/Page column 102, (2010/02/08)

The present invention relates to aniline derivatives of the general formula I or pharmaceutically acceptable salts thereof and their use.

Quinone Imine Route to Benzimidazol-2-ylcarbamates. Part 1. Synthesis of Open-chain and Cyclic 5-Acylamino Derivatives.

Rajappa, Srinivasachari,Sreenivasan, Ramaswami,Khalwadekar, Asha

, p. 1657 - 1675 (2007/10/02)

The synthesis of the N',N''-bismethoxycarbonyl-N-(4-acylaminophenyl)guanidines (4) and (7) is described.Oxidation of these with LTA has led to the benzimidazol-2-ylcarbamates. (8), (9) and (10) through a regiospecific cyclisation of quinone imine intermediates.If the acylamino group is part of a ring, the yield of benzimidazoles (15) increases with the size of the lactam ring.The direction of ring closure may be controlled by electronic and steric factors.

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