3-Iodobenzylamine hydrochloride

Name: 3-Iodobenzylamine hydrochloride
Brand: ALDRICH
Price: 363 USD
Availability: InStock

97%

Synonym(s):

(3-Iodophenyl)methanamine hydrochloride, m-Iodobenzylamine hydrochloride

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5 G

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About This Item

Linear Formula:

IC₆H₄CH₂NH₂· HCl

CAS Number:

3718-88-5

Molecular Weight:

269.51

EC Number:

223-068-5

MDL number:

MFCD00012857

UNSPSC Code:

12352100

PubChem Substance ID:

24848191

NACRES:

NA.22

Key Documents

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Quality Level

200

assay

97%

mp

188-190 °C (lit.)

SMILES string

Cl.NCc1cccc(I)c1

InChI

1S/C7H8IN.ClH/c8-7-3-1-2-6(4-7)5-9;/h1-4H,5,9H2;1H

InChI key

PYFDZOCGFHIRST-UHFFFAOYSA-N

Related Categories

Organic Building Blocks

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Show Differences

1 of 4

This Item	631337	680079	100064
Sigma-Aldrich 134996 3-Iodobenzylamine hydrochloride	Sigma-Aldrich 631337 3-Hydroxy-4-methoxybenzylamine hydrochloride	Sigma-Aldrich 680079 3-Hydroxyazetidine hydrochloride	Sigma-Aldrich 100064 3-Iodobenzylamine
assay 97%	assay 97%	assay 97%	assay 96%
Quality Level 200	Quality Level 100	Quality Level 200	Quality Level 100
mp 188-190 °C (lit.)	mp 190-195 °C (lit.)	mp 85-90 °C	mp -

Application

3-Iodobenzylamine hydrochloride was used as the starting reagent in the synthesis of N⁶-(3-iodobenzyl)-2-substituted-adenosine derivatives[1]. It was used in the synthesis of 3′-C-methyl adenosine N⁶-substituted and N⁶/C-2 disubstituted derivatives and novel 2′-C-methyl analogues[2].

pictograms

GHS08,GHS07

signalword

Danger

hcodes

H315,H317,H319,H334,H335,H361

pcodes

P201 - P280 - P302 + P352 - P305 + P351 + P338 - P308 + P313

Hazard Classifications

Eye Irrit. 2 - Repr. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number

0000462362

0000430723

0000318497

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2-Substitution of N6-benzyladenosine-5'-uronamides enhances selectivity for A3 adenosine receptors.

H O Kim et al.

Journal of medicinal chemistry, 37(21), 3614-3621 (1994-10-14)

Adenosine derivatives bearing an N6-(3-iodobenzyl) group, reported to enhance the affinity of adenosine-5'-uronamide analogues as agonists at A3 adenosine receptors (J. Med. Chem. 1994, 37, 636-646), were synthesized starting from methyl beta-D-ribofuranoside in 10 steps. Binding affinities at A1 and

Synthesis, biological evaluation, and molecular modeling of ribose-modified adenosine analogues as adenosine receptor agonists.

Loredana Cappellacci et al.

Journal of medicinal chemistry, 48(5), 1550-1562 (2005-03-04)

A number of 3'-C-methyl analogues of selective adenosine receptor agonists such as CPA, CHA, CCPA, 2'-Me-CCPA, NECA, and IB-MECA was synthesized to further investigate the subdomain of the receptor that binds the ribose moiety of the ligands. Affinity data at

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3-Iodobenzylamine hydrochloride