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About This Item
Linear Formula:
CH3C6H4CH2Cl
CAS Number:
Molecular Weight:
140.61
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-241-1
Beilstein/REAXYS Number:
507387
MDL number:
Assay:
98%
Form:
liquid
Quality Level
assay
98%
form
liquid
refractive index
n20/D 1.533 (lit.)
bp
200 °C (lit.)
mp
4 °C (lit.)
density
1.062 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
Cc1ccc(CCl)cc1
InChI
1S/C8H9Cl/c1-7-2-4-8(6-9)5-3-7/h2-5H,6H2,1H3
InChI key
DMHZDOTYAVHSEH-UHFFFAOYSA-N
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 1
flash_point_f
167.0 °F - closed cup
flash_point_c
75 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Electrophilic attack at carbon-5 of guanine nucleosides: structure and properties of the resulting guanidinoimidazole products.
R C Moschel et al.
IARC scientific publications, (70)(70), 235-240 (1986-01-01)
Małgorzata Pamuła et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 26(33), 7374-7383 (2020-02-23)
The synthesis of tetramethoxyresorcinarene podands bearing p-toluene arms connected by -SO3 - (1) and -CH2 O- (2) linkers is presented herein. In the solid state, the resorcinarene podand 1 forms an intramolecular self-inclusion complex with the pendant p-toluene group of
K Hemminki et al.
Journal of applied toxicology : JAT, 3(4), 203-207 (1983-08-01)
Benzyl chloride, benzyl bromide, p-methylbenzyl chloride, and p-nitrobenzyl chloride were used to study chemical reactivity with 4-(p-nitrobenzyl)-pyridine (NBP), and with guanosine in vitro, in relation to mutagenic potency in S. typhimurium and sister chromatid exchange (SCE) induction in CHO cells.
Global Trade Item Number
| SKU | GTIN |
|---|---|
| C73400-500G | 04061837084935 |
| C73400-5G | 04061837077326 |
| C73400-100G | 04061838353337 |

