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C73400

Sigma-Aldrich

4-Methylbenzyl chloride

98%

Synonym(s):

α-Chloro-p-xylene, p-Xylyl chloride

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About This Item

Linear Formula:
CH3C6H4CH2Cl
CAS Number:
104-82-5
Molecular Weight:
140.61
Beilstein:
507387
EC Number:
203-241-1
MDL number:
MFCD00000919
UNSPSC Code:
12352100
PubChem Substance ID:
24892958
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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Related Categories

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H302,H314

Hazard Classifications

Acute Tox. 4 Oral - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 1

Flash Point(F)

167.0 °F - closed cup

Flash Point(C)

75 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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)
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
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.
Nicholas R Oranzi et al.
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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
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