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Methyl 6-amino-5-nitropyridine-3-carboxylate is an organic compound that features a pyridine ring with a nitro group at the 5-position, an amino group at the 6-position, and a carboxylate group attached to the 3-position through a methyl ester linkage. methyl 6-amino-5-nitropyridine-3-carboxylate is characterized by its potential reactivity and functional groups, which make it a versatile intermediate in organic synthesis.

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  • 104685-75-8 Structure
  • Basic information

    1. Product Name: methyl 6-amino-5-nitropyridine-3-carboxylate
    2. Synonyms: 6-AMino-5-nitro-nicotinic acid Methyl ester;Methyl 6-aMino-5-nitropyridazine-3-carboxylate;methyl 6-amino-5-nitronicotinate;methyl 6-amino-5-nitropyridine-3-carboxylate;6-AMINO-5-NITROPYRIDINE-3-CARBOXYLIC ACID METHYL ESTER
    3. CAS NO:104685-75-8
    4. Molecular Formula: C7H7N3O4
    5. Molecular Weight: 197.149
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 104685-75-8.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.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: methyl 6-amino-5-nitropyridine-3-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 6-amino-5-nitropyridine-3-carboxylate(104685-75-8)
    11. EPA Substance Registry System: methyl 6-amino-5-nitropyridine-3-carboxylate(104685-75-8)
  • 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: 104685-75-8(Hazardous Substances Data)

104685-75-8 Usage

Uses

Used in Pharmaceutical Industry:
Methyl 6-amino-5-nitropyridine-3-carboxylate is used as a synthetic intermediate for the preparation of annulated nitrogen heterocycles, which are important in the development of pharmaceutical compounds with various therapeutic applications. The presence of the nitro and amino groups allows for further chemical modifications, enabling the synthesis of a wide range of bioactive molecules.
Used in Organic Synthesis:
In the field of organic synthesis, methyl 6-amino-5-nitropyridine-3-carboxylate serves as a key building block for the creation of complex organic molecules. Its unique structure and functional groups facilitate multiple reaction pathways, making it a valuable component in the synthesis of various organic compounds, including potential pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Research and Development:
Methyl 6-amino-5-nitropyridine-3-carboxylate is also utilized in research and development settings, where it can be employed to explore new chemical reactions, investigate the properties of novel compounds, and develop innovative synthetic methodologies. Its reactivity and structural features make it an interesting subject for academic and industrial research, potentially leading to new discoveries and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 104685-75-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,6,8 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 104685-75:
(8*1)+(7*0)+(6*4)+(5*6)+(4*8)+(3*5)+(2*7)+(1*5)=128
128 % 10 = 8
So 104685-75-8 is a valid CAS Registry Number.

104685-75-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 6-amino-5-nitropyridine-3-carboxylate

1.2 Other means of identification

Product number -
Other names methyl 2-amino-3-nitropyridine-5-carboxylate

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:104685-75-8 SDS

104685-75-8Relevant articles and documents

Novel indanyl-substituted imidazo[1,2-a]pyridines as potent reversible inhibitors of the gastric H+/K+-ATPase

Zimmermann, Peter Jan,Buhr, Wilm,Brehm, Christof,Palmer, Andreas Marc,Feth, Martin Philipp,Senn-Bilfinger, Joerg,Simon, Wolfgang-Alexander

, p. 5374 - 5378 (2007)

A series of novel 8-indanylamino- and 8-indanyloxy-substituted imidazo[1,2-a]pyridines with reduced lipophilicity was synthesized from easily accessible starting compounds. The anti-secretory activity of these compounds has been assessed in a competitive

BICYCLIC HYDROXAMIC ACIDS USEFUL AS INHIBITORS OF MAMMALIAN HISTONE DEACETYLASE ACTIVITY

-

Page/Page column 97; 98, (2017/07/14)

A compound of formula (Ia) or (Ib) or a pharmaceutically acceptable salt thereof. The compound is an inhibitor of a histone deacetylase, and as such is useful in terepy, e.g. in the treatment of autoimmune disorders, mental disorders, neurodegenerative disorders, and hyperproliferative disorders.

Phenyl-aza-benzimidazole compounds for modulating IgE and inhibiting cellular proliferation

-

, (2008/06/13)

The present invention is directed to small molecule inhibitors of the IgE response to allergens, which are useful in the treatment of allergy and/or asthma or any diseases where IgE is pathogenic. This invention also relates to phenyl-aza-benzimidazole molecules that are cellular proliferation inhibitors and thus are useful as anticancer agents. This invention further relates to small molecules which suppress cytokines and leukocytes.

Substituted triazolopyridine compounds

-

, (2008/06/13)

A compound of formula wherein R1 is —NR′R″, wherein R′ and R″ are independently selected from the group consisting of lower alkyl, —(CH2)n—C(O)NRaRb, —(CH2)n-heteroaryl, —(CH2)n-aryl, —(CH2)n—CN, —(CH2)n—O-lower alkyl or —(CH2)n-cycloalkyl, or R′ and R″ form together with the N-atom a five or six-membered non- aromatic ring, containing no or one additional heteroatom selected from the group consiting of O and S, and said ring being unsubstituted or substituted by one or two substituents, selected from the group consisting of lower alkyl, —C(O)NRaRb and —(CH2)n—O-lower alkyl, and RaRb are independently from each other hydrogen or lower alkyl; R2 is aryl or heteroaryl, unsubstituted or substituted by lower alkyl or halogen; and n is 0, 1, 2 or 3; or a pharmaceutically acceptable salt thereof. Compounds of formula I are useful in the treatment of disease associated with the adenosine A2 receptor.

Azaindenes.

-

, (2008/06/13)

The invention concerns azaindenes of the formula I (and their physiologically acceptable salts), together with pharmaceutical compositions containing them. The azaindenes antagonise the actions of angiotensin II and are of value in treating conditions suc

Benzimidazolyl-thio-tetrahydroquinolines and anti-peptic ulcer compositions containing the same

-

, (2008/06/13)

Novel tetrahydroquinoline derivatives and salts thereof and novel imidazopyridine derivatives and salts thereof, both having excellent anti-peptic ulcer activities, and are useful as treating agents for peptic ulcers such as gastric ulcer, duodenum ulcer and the like.

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