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Merck

C73400

Sigma-Aldrich

4-Methylbenzyl chloride

98%

Sinónimos:

α-Chloro-p-xylene, p-Xylyl chloride

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About This Item

Fórmula lineal:
CH3C6H4CH2Cl
Número de CAS:
Peso molecular:
140.61
Beilstein/REAXYS Number:
507387
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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

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pictograms

CorrosionExclamation mark

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

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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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
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)
Nicholas R Oranzi et al.
Analytical chemistry, 91(6), 4092-4099 (2019-02-27)
Quantitation of the serum concentration of 25-hydroxyvitamin D is a high-demand assay that suffers from long chromatography time to separate 25-hydroxyvitamin D from its inactive epimer; however, ion mobility spectrometry can distinguish the epimer pair in under 30 ms due
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.
Enis Nadia Md Yusof et al.
International journal of molecular sciences, 20(4) (2019-02-20)
Six new organotin(IV) compounds of Schiff bases derived from S-R-dithiocarbazate [R = benzyl (B), 2- or 4-methylbenzyl (2M and 4M, respectively)] condensed with 2-hydroxy-3-methoxybenzaldehyde (oVa) were synthesised and characterised by elemental analysis, various spectroscopic techniques including infrared, UV-vis, multinuclear (¹H

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