2-Chloropyridine-4-carbonyl chloride - CAS 65287-34-5

Catalog:	BB032689
Product Name:	2-Chloropyridine-4-carbonyl chloride
CAS:	65287-34-5
Synonyms:	2-chloropyridine-4-carbonyl chloride

Technical Data

Safety and Hazards

Patents

Computed Properties

IUPAC Name:	2-chloropyridine-4-carbonyl chloride
Description:	2-Chloroisonicotinoyl Chloride can be used to prepare insecticides.
Molecular Weight:	176.00
Molecular Formula:	C6H3Cl2NO
Canonical SMILES:	C1=CN=C(C=C1C(=O)Cl)Cl
InChI:	InChI=1S/C6H3Cl2NO/c7-5-3-4(6(8)10)1-2-9-5/h1-3H
InChI Key:	NPRZWOJTSGFSBF-UHFFFAOYSA-N
Boiling Point:	144-148 °C (10 mmHg)
Purity:	95 %
Density:	1.454 g/cm³
Appearance:	Colorless to yellow liquid
Storage:	Store under nitrogen
MDL:	MFCD00204232
LogP:	2.11400

Publication Number	Title	Priority Date
CN-113461732-A	3, 3-diaryl acrylate/amide compounds containing triaryl phosphonium salt and preparation method and application thereof	20210512
CN-113321595-A	Metadiamide compound and application thereof	20200228
WO-2021126999-A1	Use of biomarkers in identifying patients that will be responsive to treatment with a prmt5 inhibitor	20191217
WO-2021073373-A1	Amide compounds and preparation method therefor and use thereof	20191015
WO-2020061116-A1	Farnesoid x receptor agonists and uses thereof	20180918

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Related Functional Groups

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GHS Hazard Statement:	H301 (95.12%): Toxic if swallowed [Danger Acute toxicity, oral]
Precautionary Statement:	P260, P264, P270, P280, P301+P310, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P330, P363, P405, and P501
Signal Word:	Danger

Complexity:	140
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	174.9591691
Formal Charge:	0
Heavy Atom Count:	10
Hydrogen Bond Acceptor Count:	2
Hydrogen Bond Donor Count:	0
Isotope Atom Count:	0
Monoisotopic Mass:	174.9591691
Rotatable Bond Count:	1
Topological Polar Surface Area:	30 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	2.1