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4-(N-BOC-AMINO)-3-NITROPYRIDINE is an organic compound with the chemical formula C11H14N4O4. It is a nitro-substituted pyridine derivative that features a BOC-protected amino group. The BOC (tert-butyloxycarbonyl) group is commonly used in organic chemistry to protect amine functional groups. 4-(N-BOC-AMINO)-3-NITROPYRIDINE is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals.

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  • 623562-22-1 Structure
  • Basic information

    1. Product Name: 4-(N-BOC-AMINO)-3-NITROPYRIDINE
    2. Synonyms: 4-(N-BOC-AMINO)-3-NITROPYRIDINE;tert-Butyl (3-nitropyridin-4-yl)carbaMate
    3. CAS NO:623562-22-1
    4. Molecular Formula: C10H13N3O4
    5. Molecular Weight: 239.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 623562-22-1.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: 4-(N-BOC-AMINO)-3-NITROPYRIDINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(N-BOC-AMINO)-3-NITROPYRIDINE(623562-22-1)
    11. EPA Substance Registry System: 4-(N-BOC-AMINO)-3-NITROPYRIDINE(623562-22-1)
  • 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: 623562-22-1(Hazardous Substances Data)

623562-22-1 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
4-(N-BOC-AMINO)-3-NITROPYRIDINE is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its BOC-protected amino group allows for selective reactions and subsequent deprotection to yield the desired amine-containing products.
Used in Organic Electronics:
4-(N-BOC-AMINO)-3-NITROPYRIDINE is utilized in the development of organic light-emitting diodes (OLEDs) and materials for organic electronics. Its unique chemical structure contributes to the performance and properties of these electronic devices.
Used in Materials Science:
4-(N-BOC-AMINO)-3-NITROPYRIDINE may have potential applications in the field of materials science, where its chemical properties can be exploited to create new materials with specific characteristics.
Used as a Building Block for Complex Organic Molecules:
4-(N-BOC-AMINO)-3-NITROPYRIDINE can also serve as a building block for the synthesis of complex organic molecules, enabling the creation of a wide range of chemical compounds with diverse applications.

Check Digit Verification of cas no

The CAS Registry Mumber 623562-22-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,3,5,6 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 623562-22:
(8*6)+(7*2)+(6*3)+(5*5)+(4*6)+(3*2)+(2*2)+(1*2)=141
141 % 10 = 1
So 623562-22-1 is a valid CAS Registry Number.

623562-22-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-Butyl (3-nitropyridin-4-yl)carbamate

1.2 Other means of identification

Product number -
Other names tert-butyl N-(3-nitropyridin-4-yl)carbamate

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 -
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More Details:623562-22-1 SDS

623562-22-1Relevant articles and documents

PYRIDINE COMPOUNDS AND USES THEREOF

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Page/Page column 17; 18, (2013/03/26)

The present invention is directed to pyridine compounds of Formula (I). Separate aspects of the invention are directed to pharmaceutical compositions comprising said compounds and uses of the compounds as therapeutic agents treating neurological and psych

Preparation of substituted 1,3-dihydro-2H-imidazo[4,5-c]pyridin-2-ones

Bakke, Jan M.,Gautun, Hanna S. H.,Svensen, Harald

, p. 585 - 591 (2007/10/03)

A new synthetic route to 6-substituted-imidazo[4,5-c]pyridin-2-ons from 4-aminopyridine has been investigated. 4-Aminopyridine protected as alkyl carbamates were nitrated with dinitrogen pentoxide to the corresponding methyl, i-propyl and t-butyl 3-nitropyridin-4-yl carbamates (5a-c) in 51-63% yields. Attempts to substitute these in the 6-position by the ONSH and the VNS techniques succeeded with butylamine and the t-butyl carbamate 9. From the methyl or t-butyl 3-nitropyridin-4-yl carbamates 5a, 5c 1,3-dihydro-2H-imidazo[4,5-c]pyridin-2-one (1) was formed in 73 and 39% yields, respectively. t-Butyl 6-N-butylamin-3-aminopyridin-4-yl carbamate (6) gave 6-butylamino-1,3-dihydro-2H-imidazo[4,5-c]pyridin-2-one (7) in 53% yield.

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