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About This Item
Linear Formula:
ClC6H3(CH3)NH2
CAS Number:
Molecular Weight:
141.60
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-441-6
Beilstein/REAXYS Number:
878505
MDL number:
Assay:
98%
Form:
solid
assay
98%
form
solid
refractive index
n20/D 1.583 (lit.)
bp
241 °C (lit.)
mp
24-27 °C (lit.)
density
1.19 g/mL at 25 °C (lit.)
functional group
chloro
SMILES string
Cc1cc(Cl)ccc1N
InChI
1S/C7H8ClN/c1-5-4-6(8)2-3-7(5)9/h2-4H,9H2,1H3
InChI key
CXNVOWPRHWWCQR-UHFFFAOYSA-N
Application
4-Chloro-2-methylaniline may be used in the synthesis of the following:
- 2,8-dichloro-4,10-dimethyl-6H,12H-5,11-methanodibenzo[b,f]-diazocine via reaction with paraformaldehyde in toluene
- N-allylated derivative via palladium-catalyzed selective monoallylation with allyl alcohol
- N-(4-chloro-2-methylphenyl)benzamide via reaction with benzoyl chloride
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signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B - Muta. 2
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
255.2 °F - closed cup
flash_point_c
124 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Regulatory Information
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"Synthesis of halogen substituted analogues of Troger?s base"
Jensen J and Warnmark K
Synthesis, 2001(12), 1873-1877 (2001)
?Direct palladium-catalyzed selective monoallylation of
anilines using allylic alcohols?
anilines using allylic alcohols?
Yang C-S, et al.
Tetrahedron Letters, 41(36), 7097-7100 (2000)
"Derivatives from Isoselenocyanates: Synthesis of 2-Phenyl-6H-[5, 1, 3] benzoselenadiazocine"
Atanassov.KP, et al.
Helvetica Chimica Acta, 87(06), 1452-1466 (2004)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 590711-10G | 04061832643496 |


