Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Chemical Reagents >  Organic reagents >  Halogenated aliphatic hydrocarbons >  1-CHLORO-3-IODOPROPANE

1-CHLORO-3-IODOPROPANE

Basic information Safety Supplier Related

1-CHLORO-3-IODOPROPANE Basic information

Product Name:
1-CHLORO-3-IODOPROPANE
Synonyms:
  • 1-CHLORO-3-IODOPROPANE, 98%1-CHLORO-3-IODOPROPANE, 98%1-CHLORO-3-IODOPROPANE, 98%1-CHLORO-3-IODOPROPANE, 98%
  • 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%
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
More
Less

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.)
Flash point:
>230 °F
storage temp. 
Keep in dark place,Inert atmosphere,2-8°C
solubility 
Difficult to mix.
form 
Liquid
Specific Gravity
1.904
color 
Clear light yellow or light pink to orange
Sensitive 
Light Sensitive
BRN 
1731115
CAS DataBase Reference
6940-76-7(CAS DataBase Reference)
EPA Substance Registry System
Propane, 1-chloro-3-iodo- (6940-76-7)
More
Less

Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
8-10
TSCA 
Yes
HS Code 
29037990

MSDS

More
Less

1-CHLORO-3-IODOPROPANE Usage And Synthesis

Chemical Properties

CLEAR SLIGHTLY YELLOWISH TO LIGHT PINK LIQUID

Uses

1-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 Description

1-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.

1-CHLORO-3-IODOPROPANESupplier

Shanghai Taijilin Industrial Co., Ltd. Gold
Tel
021-021-50630626 18964684208
Email
kate@tajilin.com
Haimen Ruiyi Medical Tech Co., LTD Gold
Tel
021-54718086
Email
sales5@ruiyitech.com
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Email
jkinfo@jkchemical.com
PharmaBlock Sciences (Nanjing),Inc.
Tel
400-0255188 4000255188
Email
sales@pharmablock.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006608290; 18621169109
Email
market03@meryer.com