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4-Pyridinecarbonitrile,3-(bromomethyl)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 116986-14-2 Structure
  • Basic information

    1. Product Name: 4-Pyridinecarbonitrile,3-(bromomethyl)-(9CI)
    2. Synonyms: 4-Pyridinecarbonitrile,3-(bromomethyl)-(9CI);3-(broMoMethyl)pyridine-4-carbonitrile;3-Bromomethyl-4-cyano-pyridine
    3. CAS NO:116986-14-2
    4. Molecular Formula: C7H5BrN2
    5. Molecular Weight: 197.032
    6. EINECS: N/A
    7. Product Categories: PYRIDINE
    8. Mol File: 116986-14-2.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: 4-Pyridinecarbonitrile,3-(bromomethyl)-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Pyridinecarbonitrile,3-(bromomethyl)-(9CI)(116986-14-2)
    11. EPA Substance Registry System: 4-Pyridinecarbonitrile,3-(bromomethyl)-(9CI)(116986-14-2)
  • 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: 116986-14-2(Hazardous Substances Data)

116986-14-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116986-14-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,9,8 and 6 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 116986-14:
(8*1)+(7*1)+(6*6)+(5*9)+(4*8)+(3*6)+(2*1)+(1*4)=152
152 % 10 = 2
So 116986-14-2 is a valid CAS Registry Number.

116986-14-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(bromomethyl)pyridine-4-carbonitrile

1.2 Other means of identification

Product number -
Other names -

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:116986-14-2 SDS

116986-14-2Relevant articles and documents

HETEROCYCLIC COMPOUNDS AND USES THEREOF

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Paragraph 0371, (2021/07/31)

Provided herein are novel heterocyclic compounds, for example, compounds having Formula I, I-P, II, lI-P, or III. Also provided herein are pharmaceutical compositions comprising the compounds and methods of using the same, for example, in inhibiting aldehyde dehydrogenases and/or for treating various cancers, cancer metastasis, type 2 diabetes, pulmonary arterial hypertension (PAH) or neointimal hyperplasia (NIH).

AZAINDENOISOQUINOLINE TOPOISOMERASE I INHIBITORS

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, (2014/02/16)

The invention described herein pertains to substituted azaindenoisoquinoline compounds, in particular 7-, 8-, 9-, and 10-azaindenoisoquinoline compounds, which are inhibitors of topoisomerase I, processes and intermediates for their syntheses, pharmaceutical compositions of the compounds, and methods of using them in the treatment of cancer.

Synthesis and SAR of novel CXCR4 antagonists that are potent inhibitors of T tropic (X4) HIV-1 replication

Skerlj, Renato,Bridger, Gary,McEachern, Ernie,Harwig, Curtis,Smith, Chris,Wilson, Trevor,Veale, Duane,Yee, Helen,Crawford, Jason,Skupinska, Krystyna,Wauthy, Rossana,Yang, Wen,Zhu, Yongbao,Bogucki, David,Di Fluri, Maria,Langille, Jonathon,Huskens, Dana,De Clercq, Erik,Schols, Dominique

scheme or table, p. 262 - 266 (2011/02/27)

An early lead from the AMD070 program was optimized and a structure-activity relationship was developed for a novel series of heterocyclic containing compounds. Potent CXCR4 antagonists were identified based on anti-HIV-1 activity and Ca2+ flux

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