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2-MERCAPTO-5-NITROPYRIDINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 2127-09-5 Structure
  • Basic information

    1. Product Name: 2-MERCAPTO-5-NITROPYRIDINE
    2. Synonyms: 5-NITRO-2-PYRIDYL MERCAPTAN;5-NITRO-2-PYRIDINETHIOL;5-NITRO-2-PYRIDINETHIONE;2-MERCAPTO-5-NITROPYRIDINE;Mercaptonitropyridine;2-MERCAPTO-5-NITROPYRIDINE 98+%;5-NITRO-2-PYRIDINEETHIONE;5-Nitro-2-pyridinethiol 5-Nitro-2-pyridyl Mercaptan
    3. CAS NO:2127-09-5
    4. Molecular Formula: C5H4N2O2S
    5. Molecular Weight: 156.16
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 2127-09-5.mol
  • Chemical Properties

    1. Melting Point: 188°C
    2. Boiling Point: 220 °C at 760 mmHg
    3. Flash Point: 86.9 °C
    4. Appearance: /
    5. Density: 1.48 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 7.09±0.20(Predicted)
    10. CAS DataBase Reference: 2-MERCAPTO-5-NITROPYRIDINE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-MERCAPTO-5-NITROPYRIDINE(2127-09-5)
    12. EPA Substance Registry System: 2-MERCAPTO-5-NITROPYRIDINE(2127-09-5)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 26-36/37/39-36
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 2127-09-5(Hazardous Substances Data)

2127-09-5 Usage

Synthesis Reference(s)

Tetrahedron Letters, 34, p. 939, 1993 DOI: 10.1016/S0040-4039(00)77459-4

Check Digit Verification of cas no

The CAS Registry Mumber 2127-09-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,2 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2127-09:
(6*2)+(5*1)+(4*2)+(3*7)+(2*0)+(1*9)=55
55 % 10 = 5
So 2127-09-5 is a valid CAS Registry Number.

2127-09-5SDS

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 5-nitro-1H-pyridine-2-thione

1.2 Other means of identification

Product number -
Other names 5-Nitropyridine-2-thiol

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:2127-09-5 SDS

2127-09-5Relevant articles and documents

Peptide Tethering: Pocket-Directed Fragment Screening for Peptidomimetic Inhibitor Discovery

Arora, Paramjit S.,Marrone, Frank,Modell, Ashley E.,Panigrahi, Nihar R.,Zhang, Yingkai

supporting information, p. 1198 - 1204 (2022/02/05)

Constrained peptides have proven to be a rich source of ligands for protein surfaces, but are often limited in their binding potency. Deployment of nonnatural side chains that access unoccupied crevices on the receptor surface offers a potential avenue to

A coordinated synthesis and conjugation strategy for the preparation of homogeneous glycoconjugate vaccine candidates

Grayson, Elizabeth J.,Bernardes, Goncalo J. L.,Chalker, Justin M.,Boutureira, Omar,Koeppe, Julia R.,Davis, Benjamin G.

supporting information; experimental part, p. 4127 - 4132 (2011/07/07)

A sweet solution: A strategy for the synthesis of well-defined carbohydrate-based vaccines is presented. The approach couples complex oligosaccharide synthesis to site-specific conjugation methodology to provide pure glycoprotein vaccine candidates (see scheme). Copyright

Heteroaryl thioglycosides, a new class of substrates for glycosidases

Niemiec-Cyganek,Szeja

, p. 969 - 973 (2007/10/03)

We have found that heteroaryl thioglycosides are useful substrates of β-glucosidase from almond and can act as a new class of donors in transglycosylation reaction.

PYRANONE COMPOUNDS USEFUL TO TREAT RETROVIRAL INFECTIONS

-

, (2008/06/13)

The present invention relates to compounds of formulae (I) and (II) which are pyran-2-ones, 5,6-dihydro-pyran-2-ones, 4-hydroxy-benzopyran-2-ones, 4-hydroxy-cycloalkyl[b]pyran-2-ones, and derivatives thereof, useful for inhibiting a retrovirus in a mammalian cell infected with said retrovirus, wherein R 10 and R 20 taken together are formulae (III) and (IV). STR1

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