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1-CHLORO-3-IODOPROPANE

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1-CHLORO-3-IODOPROPANE manufacturers
1-CHLORO-3-IODOPROPANE Basic information
Product Name:1-CHLORO-3-IODOPROPANE
Synonyms:1-chloro-3-iodo-propan;3-CHLOROPROPYL IODIDE;1-CHLORO-3-IODOPROPANE;TRIMETHYLENE CHLOROIODIDE;1-Chloro-3-iodoproprane;1-CHLORO-3-IODOPROPANE, STAB.;1-Chloro-3-iodopropane,98%;1-CHLORO-3-IODOPROPANE , STABILIZED WITH COPPER
CAS:6940-76-7
MF:C3H6ClI
MW:204.44
EINECS:230-088-8
Product Categories:omega-Functional Alkanols, Carboxylic Acids, Amines & Halides;omega-Haloalkyl Chlorides
Mol File:6940-76-7.mol
1-CHLORO-3-IODOPROPANE Structure
1-CHLORO-3-IODOPROPANE Chemical Properties
Boiling point 170-172 °C (lit.)
density 1.904 g/mL at 25 °C (lit.)
vapor density 6.8 (vs air)
vapor pressure 2 mm Hg ( 20 °C)
refractive index n20/D 1.548(lit.)
Fp >230 °F
storage temp. Keep in dark place,Inert atmosphere,2-8°C
solubility Difficult to mix.
form Liquid
Specific Gravity1.904
color Clear light yellow or light pink to orange
Sensitive Light Sensitive
BRN 1731115
InChI1S/C3H6ClI/c4-2-1-3-5/h1-3H2
InChIKeySFOYQZYQTQDRIY-UHFFFAOYSA-N
SMILESClCCCI
CAS DataBase Reference6940-76-7(CAS DataBase Reference)
EPA Substance Registry SystemPropane, 1-chloro-3-iodo- (6940-76-7)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
F 8-10
TSCA TSCA listed
HS Code 29037990
Storage Class10 - Combustible liquids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
1-CHLORO-3-IODOPROPANE Usage And Synthesis
Chemical PropertiesCLEAR SLIGHTLY YELLOWISH TO LIGHT PINK LIQUID
Uses1-Chloro-3-iodopropane has been used in the synthesis of N-[4-[5-(2,4-diamino-6-oxo-1,6-dihydropyrimidin-5-yl)-2-(2,2,2-trifluoroacetyl)pentyl]benzoyl]-L-glutamic acid, an inhibitor of glycinamide ribonucleotide transformylase (GAR Tfase) and aminoimidazole carboxamide ribonucleotide transformylase (AICAR Tfase), interesting proton sponge type molecule quino[7,8-h]quinoline.
General Description1-Chloro-3-iodopropane undergoes asymmetric α-alkylation with N-sulfinyl imidates to yield 2-substituted N-tert-butanesulfinyl-5-chloropentanimidates. Electroreduction of 1-chloro-3-iodopropane at glassy carbon electrode in dimethylformamide containing tetra-n-butylammonium perchlorate has been investigated by cyclic voltammetry. It also participates in conjugate addition of alkyl iodides to α,β-unsaturated nitriles in water.
Tag:1-CHLORO-3-IODOPROPANE(6940-76-7) Related Product Information
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