164771
3-Aminobenzonitrile
99%
Synonym(s):
3-Cyanoaniline
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| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 5 g | Check Cart for Availability | $58.80 |
About This Item
Linear Formula:
H2NC6H4CN
CAS Number:
Molecular Weight:
118.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
218-800-5
Beilstein/REAXYS Number:
636498
MDL number:
Assay:
99%
Form:
solid
assay
99%
form
solid
mp
48-53 °C (lit.)
functional group
nitrile
SMILES string
Nc1cccc(c1)C#N
InChI
1S/C7H6N2/c8-5-6-2-1-3-7(9)4-6/h1-4H,9H2
InChI key
NJXPYZHXZZCTNI-UHFFFAOYSA-N
General description
3-Aminobenzonitrile on condensation reaction with 4-isothiocyanato-4-methyl pentane-2-one gives condensed monocyclic pyrimidine derivatives[1].
1 of 1
This Item | |||
|---|---|---|---|
| assay 99% | assay 99% | assay 98% | assay 98% |
| Quality Level 100 | Quality Level 100 | Quality Level 200 | Quality Level 100 |
| mp 48-53 °C (lit.) | mp 92-94 °C (lit.) | mp 45-48 °C (lit.) | mp 83-85 °C (lit.) |
| form solid | form solid | form crystals | form solid |
| functional group nitrile | functional group phenyl | functional group - | functional group - |
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Skin Sens. 1
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
233.6 °F - closed cup
flash_point_c
112 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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Cheng Hua Jin et al.
European journal of medicinal chemistry, 46(9), 3917-3925 (2011-06-24)
A series of 1-substituted-3(5)-(6-methylpyridin-2-yl)-4-(quinoxalin-6-yl)pyrazoles 14a-d, 15a-d, 17a, 17b, 18a-d, 19a, and 19b has been synthesized and evaluated for their ALK5 inhibitory activity in an enzyme assay and in a cell-based luciferase reporter assay. The 2-[3-(6-methylpyridin-2-yl)-4-(quinoxalin-6-yl)-1H-pyrazol-1-yl]-N-phenylethanethioamide (18a) inhibited ALK5 phosphorylation with
Jeffrey C Pelletier et al.
Bioorganic & medicinal chemistry, 13(21), 5986-5995 (2005-08-16)
An unusual combination of Weinreb amidation and Mitsunobu lactam formation was used to prepare highly substituted gamma-lactam analogues of a thiazolidinone follicle stimulating hormone receptor agonist. The analogue synthesis was stereoselective and the final products were chemically stable. Biological properties
Sham M Sondhi et al.
Bioorganic & medicinal chemistry, 13(22), 6158-6166 (2005-08-24)
3-Aminobenzonitrile and 2-amino-4-phenyl thiazole on condensation with 4-isothiocyanato-4-methyl pentane-2-one gave condensed monocyclic pyrimidine derivatives 1 and 2, 3, respectively. Condensation of 3-aminopropyl imidazole with 3-isothiocyantobutanal gave condensed monocyclic pyrimidine derivative 4. Bicyclic pyrimidine derivatives 5a and 5b have been synthesized
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 164771-25G | 04061838748317 |
| 164771-5G | 04061832098425 |