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6940-76-7

6940-76-7 | 1-Chloro-3-iodopropane

CAS No: 6940-76-7 Catalog No: AG0032QQ MDL No:MFCD00001096

Product Description

Catalog Number:
AG0032QQ
Chemical Name:
1-Chloro-3-iodopropane
CAS Number:
6940-76-7
Molecular Formula:
C3H6ClI
Molecular Weight:
204.4372
MDL Number:
MFCD00001096
IUPAC Name:
1-chloro-3-iodopropane
InChI:
InChI=1S/C3H6ClI/c4-2-1-3-5/h1-3H2
InChI Key:
SFOYQZYQTQDRIY-UHFFFAOYSA-N
SMILES:
ClCCCI
EC Number:
230-088-8
NSC Number:
60189

Properties

Complexity:
16.4  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
203.92g/mol
Formal Charge:
0
Heavy Atom Count:
5  
Hydrogen Bond Acceptor Count:
0
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
204.435g/mol
Monoisotopic Mass:
203.92g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
0A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.3  

Literature

Title Journal
Total synthesis of (-)-kopsinine by an asymmetric one-pot [n+2+3] cyclization. Chemistry, an Asian journal 20121001
Have regulatory efforts to reduce organophosphorus insecticide exposures been effective? Environmental health perspectives 20120401
Urinary concentrations of dialkylphosphate metabolites of organophosphorus pesticides: National Health and Nutrition Examination Survey 1999-2004. International journal of environmental research and public health 20110801
Asymmetric synthesis of chiral N-sulfinyl 3-alkyl- and 3-arylpiperidines by α-alkylation of N-sulfinyl imidates with 1-chloro-3-iodopropane. The Journal of organic chemistry 20110107
Synthesis of crispine A analogues via an intramolecular Schmidt reaction. Beilstein journal of organic chemistry 20070101
Measurement of human urinary organophosphate pesticide metabolites by automated solid-phase extraction derivation and gas chromatography-tandem mass spectromy. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences 20061020
Synthesis and biological evaluation of N-[4-[5-(2,4-diamino-6-oxo-1,6-dihydropyrimidin-5-yl)-2-(2,2,2-trifluoroacetyl)pentyl]benzoyl]-L-glutamic acid as a potential inhibitor of GAR Tfase and the de novo purine biosynthetic pathway. Bioorganic & medicinal chemistry 20050516

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