Name: Name:3-Iodoaniline
Brand: AABLOCKS
SKU: AA0033NO
Rating: 90 (10 reviews)

Technical Information

Catalog Number: AA0033NO

Chemical Name: 3-Iodoaniline

CAS Number: 626-01-7

Molecular Formula: C6H6IN

Molecular Weight: 219.0230

MDL Number: MFCD00007781

SMILES: Nc1cccc(c1)I

NSC Number: 34545

Properties

BP: 271.6°C at 760 mmHg

Form: Solid

MP: 21-24 °C

Refractive Index: n20/D 1.682(lit.)

Stability: Light Sensitive

Storage: Inert atmosphere;2-8℃;

Complexity: 74.9

Covalently-Bonded Unit Count: 1

Heavy Atom Count: 8

Hydrogen Bond Acceptor Count: 1

Hydrogen Bond Donor Count: 1

XLogP3: 1.7

Literature fold

Title: (E)-1-[(3-Iodo-phen-yl)imino-meth-yl]naphthalen-2-ol.

Journal: Acta crystallographica. Section E, Structure reports online20121001

Title: Application of ynamides in the synthesis of 2-amidoindoles.

Journal: Organic letters20090101

Title: Radioiodination of humic substances via azocoupling with 3-[125I] iodoaniline.

Journal: Environmental science & technology20080601

Title: Ionic-liquid-promoted palladium-catalyzed multicomponent cyclocarbonylation of o-iodoanilines and allenes to form methylene-2,3-dihydro-1H-quinolin-4-ones.

Journal: The Journal of organic chemistry20070427

Title: 3-iodoanilinium 2-carboxy-6-nitrobenzoate: a three-dimensional framework built from O-H...O and N-H...O hydrogen bonds and a two-centre iodo-nitro interaction.

Journal: Acta crystallographica. Section C, Crystal structure communications20050401

Title: Concise synthesis of (+/-)-horsfiline and (+/-)-coerulescine by tandem cyclisation of iodoaryl alkenyl azides.

Journal: Organic & biomolecular chemistry20030107

Title: Synthesis of novel alpha-C-glycosylamino acids and reverse regioselectivity in Larock's heteroannulation for the synthesis of the indole nucleus.

Journal: Bioscience, biotechnology, and biochemistry20021001

626-01-7 | 3-Iodoaniline