ChemicalBook > CAS DataBase List > 2-IODO-1H-INDOLE

2-IODO-1H-INDOLE

Product Name
2-IODO-1H-INDOLE
CAS No.
26340-49-8
Chemical Name
2-IODO-1H-INDOLE
Synonyms
2-IODO-1H-INDOLE;1H-Indole,2-iodo-
CBNumber
CB62454849
Molecular Formula
C8H6IN
Formula Weight
243.04
MOL File
26340-49-8.mol
More
Less

2-IODO-1H-INDOLE Property

Melting point:
79-81 °C
Boiling point:
341.7±15.0 °C(Predicted)
Density 
1.960±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
solubility 
Chloroform (Slightly), DMSO (Slightly)
form 
solid
pka
15.57±0.30(Predicted)
color 
Brown
More
Less

Safety

HS Code 
2933998090
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

More
Less

N-Bromosuccinimide Price

TRC
Product number
I707390
Product name
2-Iodoindole
Packaging
250mg
Price
$150
Updated
2021/12/16
TRC
Product number
I707390
Product name
2-Iodoindole
Packaging
2.5g
Price
$1190
Updated
2021/12/16
AK Scientific
Product number
2333AB
Product name
2-Iodo-1H-indole
Packaging
5g
Price
$1738
Updated
2021/12/16
Medical Isotopes, Inc.
Product number
70924
Product name
2-Iodoindole
Packaging
10g
Price
$2200
Updated
2021/12/16
AK Scientific
Product number
2333AB
Product name
2-Iodo-1H-indole
Packaging
250mg
Price
$320
Updated
2021/12/16
More
Less

2-IODO-1H-INDOLE Chemical Properties,Usage,Production

Uses

2-Iodoindole is used in the synthesis of arylthioindole molecules as a class of tubulin polymerization inhibitors. Also used in the synthesis of combretastatin A-4 derivatives.

Synthesis

120-72-9

26340-49-8

General procedure for the synthesis of 2-iodoindole from indole: n-butyllithium (nBuLi, 17 mL, 2.62 M hexane solution, 44.54 mmol) was slowly added to a tetrahydrofuran (THF, 80 mL) solution of indole (5.00 g, 42.68 mmol) at -78 °C. The resulting white suspension was stirred at -78 °C for 0.5 h and then bubbled through carbon dioxide (CO2, gas) for 10 min. The solvent was evaporated at 0 °C (~20 lHPa), the crystalline residue was dissolved in THF (100 mL) and cooled to -78 °C, and tert-butyllithium (tBuLi, 31 mL, 1.46 M pentane solution, 45.26 mmol) was added dropwise. After stirring at -78 °C for 1 h, a THF (80 mL) solution of 1,2-diiodoethane (14.40 g, 51.09 mmol) was added dropwise. Stirring was continued at -78 °C for 1 h. Water (H2O, 5 mL) was then added dropwise and the reaction mixture was slowly warmed to room temperature. The reaction was quenched with saturated aqueous ammonium chloride (NH4Cl, 50 mL). The organic and aqueous layers were separated and the aqueous layer was extracted with ethyl acetate (AcOEt, 2 x 80 mL). The organic layers were combined and washed sequentially with 20% sodium thiosulfate (Na2S2O3, 80 mL) aqueous solution, brine (80 mL), dried with anhydrous magnesium sulfate (MgSO4) and concentrated under reduced pressure. The residue was purified by recrystallization from hexane/dichloromethane (70:1, 40 mL) to afford 2-iodoindole (7.62 g, 74% yield) as white crystals. The filtrate was concentrated under reduced pressure and the residue was purified by recrystallization from hexane/dichloromethane (70:1, 10 mL) to afford 2-iodoindole (0.56 g, 5% yield) as white crystals. The filtrate was again concentrated under reduced pressure and the residue was purified by recrystallization from hexane/dichloromethane (70:1, 8 mL) to afford 2-iodoindole (0.27 g, 3% yield) as light purple crystals. Finally, the filtrate was concentrated under reduced pressure and the residue was purified by fast chromatography (silica gel, hexane/ethyl acetate = 35:1) to afford 2-iodoindole (0.42 g, 4% yield) as white crystals.The total yield of 2-iodoindole was 86%.

References

[1] Tetrahedron Letters, 1997, vol. 38, # 44, p. 7661 - 7664
[2] Tetrahedron, 2001, vol. 57, # 24, p. 5199 - 5212
[3] Tetrahedron Letters, 2001, vol. 42, # 16, p. 2949 - 2951
[4] Tetrahedron Letters, 2007, vol. 48, # 10, p. 1805 - 1808
[5] Tetrahedron, 2013, vol. 69, # 45, p. 9481 - 9493

2-IODO-1H-INDOLE Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

2-IODO-1H-INDOLE Suppliers

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
Country
China
ProdList
42934
Advantage
64
Heterochem
Tel
027-88041443 13072715837
Fax
027-51829379
Email
sales@hetero-chem.com
Country
China
ProdList
696
Advantage
58
Wuhan TCASChem Technology Co., Ltd.
Tel
027-86697669 13986148687
Fax
86-027-86697669
Email
sales@tcaschem.com
Country
China
ProdList
3993
Advantage
55
Shanghai Raise Chemical Technology Co.,Ltd
Tel
+86-021-50935922
Fax
+86-021-33847795
Country
China
ProdList
7865
Advantage
55
Shanghai Run-Biotech Co., Ltd.
Tel
021-57171705 13817537615
Fax
QQ3095748324
Email
sales@run-biotech.com
Country
China
ProdList
2338
Advantage
58
Bide Pharmatech Ltd.
Tel
400-164-7117 13681763483
Fax
+86-21-61629029
Email
product02@bidepharm.com
Country
China
ProdList
39966
Advantage
60
Shenzhen Gre-syn Chemical Technology Co., Ltd.
Tel
0755-0755-89366401 18617066401
Fax
-
Email
hangbingfang@163.com
Country
China
ProdList
951
Advantage
55
Hangzhou Milestone Pharmtech Co., Ltd.
Tel
0571-82896630 18969958410
Email
sales_hz@milestonepharmtech.com
Country
China
ProdList
4894
Advantage
55
Shanghai YuanYe Biotechnology Co., Ltd.
Tel
021-61312847; 18021002903
Fax
QQ:3008007432
Email
3008007409@qq.com
Country
China
ProdList
71826
Advantage
60
More
Less

View Lastest Price from 2-IODO-1H-INDOLE manufacturers

Career Henan Chemical Co
Product
2-IODO-1H-INDOLE 26340-49-8
Price
US $1.00/KG
Min. Order
1g
Purity
98%min
Supply Ability
ask
Release date
2019-12-20

26340-49-8, 2-IODO-1H-INDOLERelated Search:


  • 2-IODO-1H-INDOLE
  • 1H-Indole,2-iodo-
  • 26340-49-8