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Home > Encyclopedia > 6-Chloro-2-pyridinecarbonitrile

6-Chloro-2-pyridinecarbonitrile

6-Chloro-2-pyridinecarbonitrile structure

6-Chloro-2-pyridinecarbonitrile 

structure
  • CAS No:

    33252-29-8

  • Formula:

    C6H3ClN2

  • Chemical Name:

    6-Chloro-2-pyridinecarbonitrile

  • Synonyms:

    2-Pyridinecarbonitrile,6-chloro-;Picolinonitrile,6-chloro-;6-Chloro-2-pyridinecarbonitrile;2-Chloro-6-cyanopyridine;6-Chloropyridine-2-carbonitrile;2-Chloropyridine-6-carbonitrile;6-Chloropicolinonitrile

  • Categories:

    Pharmaceutical Intermediates  >  Heterocyclic Compound

Description

Off-white Cryst

6-Chloro-2-pyridinecarbonitrile Basic Attributes

138.55

138.55

251-429-7

ZS4YVY14OF

DTXSID40186897

2933399090

Characteristics

36.7

1.9

Off-white Cryst

1.3±0.1 g/cm3

86-88 °C

245.3ºC at 760 mmHg

102.1±21.8 °C

1.566

Safety Information

III

6.1

UN 2811 6.1/PG 3

3

22-37/38-41-36/37/38

26-36/37/39-37

Xn,T,Xi

P261-P280-P301 + P310-P305 + P351 + P338

H301-H315-H318-H335

|Danger|H301 (91.3%): Toxic if swallowed [Danger Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P310, P302+P352, P304+P340, P305+P351+P338, P310, P312, P321, P322, P330, P332+P313, P337+P313, P361, P362, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 46 companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

6-Chloro-2-pyridinecarbonitrile Use and Manufacturing

Methods of Manufacturing

(2) The following may be mentioned as preferred compounds of the general formula (I) which can be prepared by the process according to the invention: 2, 3-dichloropyridine 2, 4-dichloropyridine 2, 6-dichloropyridine 2-chloro-3-cyano-pyridine 2-chloro-6-cyano-pyridine methyl 6-chloro-pyridine-2-carboxylate ethyl 6-chloro-pyridine-2-carboxylate N, N-dimethyl-6-chloro-pyridine-2-carboxamide N, N-diethyl-6-chloro-pyridine-2-carboxamide ...The following may be mentioned as compounds of the general formula (I) which can preferably be prepared using the process according to the invention: 2, 3-Dichloropyridine 2, 4-Dichloropyridine 2, 6-Dichloropyridine 2-Chloro-3-cyano-pyridine 2-Chloro-6-cyano-pyridine Methyl 6-chloro-pyridine-2-carboxylate Ethyl 6-chloro-pyridine-2-carboxylate N, N-Dimethyl-6-chloro-pyridine-2-carboxamide N, N-Diethyl-6-chloro-pyridine-2-carboxamide ...Under an argon stream, N- (4-phenylbenzoyl) benzamidine (300 mg, 1.0 mmol), The title compound of this step is prepared by the method described in the first step of Example 1, That is, 2-(4-Boc-piperazin-1-yl)pyrimidine-5-boronic acid pinacol ester (2.70 g, 6.93 mmol), The title compound of this step was prepared by the method described in Example 1, Step 1, namely, 2-[4-(Boc)piperazin-1-yl]pyrimidine-5-boronic acid pinacol ester (2.70 g, 6.93 mmol),

Uses

It can be used as substrate for Negishi coupling reaction with aryl zinc halide catalyzed by Pd-NHC (PEPPSI-Ipr, catalog number 668032).

Computed Properties

Molecular Weight:138.55
XLogP3:1.9
Hydrogen Bond Acceptor Count:2
Exact Mass:137.9984758
Monoisotopic Mass:137.9984758
Topological Polar Surface Area:36.7
Heavy Atom Count:9
Complexity:137
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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