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Methyl 4-amino-3-bromo-5-nitrobenzenecarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 105655-17-2 Structure
  • Basic information

    1. Product Name: Methyl 4-amino-3-bromo-5-nitrobenzenecarboxylate
    2. Synonyms: 2-Bromo-4-(methoxycarbonyl)-6-nitroaniline, 2-Amino-3-bromo-5-(methoxycarbonyl)nitrobenzene
    3. CAS NO:105655-17-2
    4. Molecular Formula: C8H7BrN2O4
    5. Molecular Weight: 275.05618
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 105655-17-2.mol
  • Chemical Properties

    1. Melting Point: 107-109℃
    2. Boiling Point: 408.5±40.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.744±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: -4.79±0.25(Predicted)
    10. CAS DataBase Reference: Methyl 4-amino-3-bromo-5-nitrobenzenecarboxylate(CAS DataBase Reference)
    11. NIST Chemistry Reference: Methyl 4-amino-3-bromo-5-nitrobenzenecarboxylate(105655-17-2)
    12. EPA Substance Registry System: Methyl 4-amino-3-bromo-5-nitrobenzenecarboxylate(105655-17-2)
  • 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: 105655-17-2(Hazardous Substances Data)

105655-17-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105655-17-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,6,5 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 105655-17:
(8*1)+(7*0)+(6*5)+(5*6)+(4*5)+(3*5)+(2*1)+(1*7)=112
112 % 10 = 2
So 105655-17-2 is a valid CAS Registry Number.

105655-17-2 Well-known Company Product Price

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  • Alfa Aesar

  • (H33216)  Methyl 4-amino-3-bromo-5-nitrobenzoate, 97%   

  • 105655-17-2

  • 1g

  • 758.0CNY

  • Detail
  • Alfa Aesar

  • (H33216)  Methyl 4-amino-3-bromo-5-nitrobenzoate, 97%   

  • 105655-17-2

  • 5g

  • 2475.0CNY

  • Detail

105655-17-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-amino-3-bromo-5-nitrobenzoate

1.2 Other means of identification

Product number -
Other names methylaminobromonitrobenzenecarboxylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:105655-17-2 SDS

105655-17-2Relevant articles and documents

Synthesis of 3,5,7-substituted indoles via heck cyclisation

Charrier, Nicolas,Demont, Emmanuel,Dunsdon, Rachel,Maile, Graham,Naylor, Alan,O'Brien, Alistair,Redshaw, Sally,Theobald, Pam,Vesey, David,Walter, Daryl

, p. 3071 - 3074 (2005)

Traditional strategies in indole chemistry do not allow high yielding access to some substitution patterns such as 3,5,7-trisubstituted indoles. We report in this article the efficient synthesis of this type of indole. The Heck cyclisation strategy we use

STING PYRAZOLE AGONISTS AND USES THEREOF

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Paragraph 00353, (2020/07/14)

The present invention provides compounds, compositions thereof, and methods of using the same for the modulation of STING, and the treatment of STING-mediated disorders.

P2X3, RECEPTOR ANTAGONISTS FOR TREATMENT OF PAIN

-

Page/Page column 88, (2010/11/18)

The subject invention relates to novel P2X3 receptor antagonists that play a critical role in treating disease states associated with pain, in particular peripheral pain, inflammatory pain, or tissue injury pain that can be treated using a P2X3 receptor subunit modulator.

Synthesis of indoles: Efficient functionalisation of the 7-position

Charrier, Nicolas,Demont, Emmanuel,Dunsdon, Rachel,Maile, Graham,Naylor, Alan,O'Brien, Alistair,Redshaw, Sally,Theobald, Pam,Vesey, David,Walter, Daryl

, p. 3467 - 3477 (2008/02/10)

Traditional strategies in indole chemistry do not allow high-yielding access to some substitution patterns such as 3,5,7-trisubstituted indoles. We report in this article the efficient synthesis of this type of indole. The Heck cyclisation strategy we use

TRICYCLIC INDOLE DERIVATIVES FOR USE IN THE TREATMENT OF ALZHEIMER’S DISEASE

-

Page/Page column 19, (2010/11/08)

The present invention relates to novel ketone compounds of formula (I) having Asp2 (β-secretase, BACE1 or Memapsin-2) inhibitory activity, processes for their preparation, to compositions containing them and to their use in the treatment of diseases chara

TRICYCLIC INDOLE DERIVATIVES AND THEIR USE IN THE TREATMENT OF ALZHEIMER’S DISEASE

-

Page 16, (2010/02/09)

The present invention relates to novel hydroxyethylamine compounds having Asp2 (β-secretase, BACE1 or Memapsin) inhibitory activity, processes for their preparation, to compositions containing them and to their use in the treatment of diseases characterised by elevated β- amyloid levels or β-amyloid deposits, particularly Alzheimer's disease.

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