696-40-2

Basic information

• Product Name: 3-Iodobenzylamine
• Synonyms: AURORA KA-7711;3-IODOBENZYLAMINE;RARECHEM AL BW 0705;3-Iodobenzylamine,97%;3-IODOBENZYLAE;3-Iodobenzenemethanamine;3-IodobenzylaMine, 97% 1GR;(3-iodophenyl)MethanaMine
• CAS NO: 696-40-2
• Molecular Formula: C₇H₈IN
• Molecular Weight: 233.05
• EINECS: -0
• Product Categories: Amines;C7;Nitrogen Compounds
• Mol File: 696-40-2.mol
• Article Data: 8

Chemical Properties

• Melting Point: 248-249 °C(Solv: N,N-dimethylformamide (68-12-2))
• Boiling Point: 132 °C8 mm Hg(lit.)
• Flash Point: >230 °F
• Appearance: Clear light yellow/Liquid
• Density: 1.748 g/mL at 25 °C(lit.)
• Refractive Index: 1.638-1.64
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• PKA: 8.79±0.10(Predicted)
• Water Solubility: Difficult to mix in water.
• Sensitive: Air & Light Sensitive
• BRN: 2689602
• CAS DataBase Reference: 3-Iodobenzylamine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Iodobenzylamine(696-40-2)
• EPA Substance Registry System: 3-Iodobenzylamine(696-40-2)

Safety Data

• Hazard Codes: Xn
• Statements: 36/37/38-42/43-63
• Safety Statements: 23-26-36/37/39
• RIDADR: 2735
• WGK Germany: 3
• HazardClass: 8
• PackingGroup: II
• Hazardous Substances Data: 696-40-2(Hazardous Substances Data)

Usage

Chemical Properties

clear light yellow liquid

Uses

It is a pharmaceutical intermediate.

InChI:InChI=1/C7H8IN/c8-7-3-1-2-6(4-7)5-9/h1-4H,5,9H2

Upstream product

• 200706-60-1 N-(3-iodobenzyl)phthalimide 
• 625-95-6 3-Iodotoluene 
• 49617-83-6 m-Iodobenzyl bromide 
• 69113-59-3 3-iodobenzonitrile 
• 60076-09-7 1-(chloromethyl)-3-iodobenzene 

Downstream Products

• 104291-06-7 N-[(3-iodophenyl)methyl]acetamide 
• 80664-11-5 (3-iodo-benzyl)-urea 
• 54364-37-3 (3-Iodo-benzyl)-dimethyl-amine; hydrochloride 
• 696-41-3 m-iodobenzaldehyde 
• 194154-35-3 (S)-3-(9H-Fluoren-9-ylmethoxycarbonylamino)-N-(3-iodo-benzyl)-succinamic acid tert-butyl ester 

Relevant articles and documents

(3-(1H-1,2,3-triazole)phenyl)phosphoric acid derivative as well as preparation method and application thereof

The invention relates to the technical field of medicinal chemistry, and discloses a (3-(1H-1,2,3-triazole)phenyl)phosphoric acid derivative derivative as shown in a formula X which is described in the specification. The derivative has good and broad-spec

Quadruple π stack of two perylene bisimide tweezers: A bimolecular complex with kinetic stability

Self-assembly: A tweezer-type perylene bisimide (PBI) dyad self-assembles into a defined bimolecular complex composed of a quadruple PBI π stack with remarkable kinetic stability, which is unprecedented for π-stacked dye aggregates (see picture). These persistent supramolecular species are of considerable interest for the elucidation of functional properties of dye aggregates. Copyright

ARYL FLUOROETHYL UREAS ACTING AS ALPHA 2 ADRENERGIC AGENTS

The invention provides well-defined aryl fluoroethyl ureas that are useful as selective alpha2 adrenergic agonists. As such, the compounds described herein are useful in treating a wide variety of disorders associated with modulation of alpha2 adrenergic receptors.