3-Iodophenylboronic acid

CAS No.：221037-98-5

Important Notice

This product is a chemical product/pharmaceutical intermediate. It is not a drug, an active pharmaceutical ingredient (API), or a pharmaceutical-grade material. It has not been granted a drug approval number or a Chemical Drug Substance Approval Notice, has not passed drug-related review and approval, and is not manufactured, tested, or released in accordance with pharmaceutical GMP.
This product is intended solely for non-clinical research, process development, quality studies, further chemical processing, or chemical synthesis. It must not be used in drug-product manufacturing, clinical trials, clinical diagnosis, or administration to humans or animals, or be sold, used as an input, submitted for regulatory filing, or released as an API or pharmaceutical material.
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3-Iodophenylboronic acid Basic information

Product Name:	3-Iodophenylboronic acid
Synonyms:	3-IODOPHENYLBORONIC ACID;RARECHEM AH PB 0036;3-Iodophenylboronic;3-Iodophenylboronic acid,97%;3-Iodophenylboronic acid ,98%;3-Iodophenylboronic acid, May contain varying amounts of anhydride, 97%;3-Iodophenylboronic acid, 97%, May contain varying aMounts of anhydride;Boronic acid, B-(3-iodophenyl)-
CAS:	221037-98-5
MF:	C6H6BIO2
MW:	247.83
EINECS:
Product Categories:	Aryl;Boronic Acids;Boronic Acids and Derivatives;Boronic Acids
Mol File:	221037-98-5.mol

3-Iodophenylboronic acid Chemical Properties

Melting point	195-197 °C (lit.)
Boiling point	358.8±44.0 °C(Predicted)
density	1.95±0.1 g/cm3(Predicted)
storage temp.	Keep in dark place,Sealed in dry,Room Temperature
form	solid
pka	7.67±0.10(Predicted)
Sensitive	Light Sensitive
CAS DataBase Reference	221037-98-5(CAS DataBase Reference)

Safety Information

Hazard Codes	Xn
Risk Statements	22-36/37/38
Safety Statements	26-36-37/39
WGK Germany	3
HS Code	29319090

MSDS Information

Provider	Language
ACROS	English
SigmaAldrich	English

3-Iodophenylboronic acid Usage And Synthesis

Chemical Properties	White to light yellow crystal powde
Uses	Reactant involved in: Aerobic oxidative coupling with arenes Coupling with acetals Synthesis of inhibitors of homoserine transacetylase Boron-Heck arylation with alkenes N-arylation Heck reactions with electrophilic alkenes

3-Iodophenylboronic acid Preparation Products And Raw materials

Raw materials

1,3-DIIODOBENZENE-->Tributyl borate

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