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328987

Sigma-Aldrich

Phenyl chlorodithioformate

95%

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About This Item

Linear Formula:
ClCS2C6H5
CAS Number:
16911-89-0
Molecular Weight:
188.70
MDL number:
MFCD00013429
UNSPSC Code:
12352100
PubChem Substance ID:
24859763
NACRES:
NA.22

Quality Level

100

Assay

95%

form

liquid

refractive index

n20/D 1.6688 (lit.)

bp

135 °C/15 mmHg (lit.)

density

1.331 g/mL at 25 °C (lit.)

functional group

chloro
thioether

storage temp.

2-8°C

SMILES string

ClC(=S)Sc1ccccc1

InChI

1S/C7H5ClS2/c8-7(9)10-6-4-2-1-3-5-6/h1-5H

InChI key

XEXIHCWFFNGQDE-UHFFFAOYSA-N

General description

Kinetics and mechanism of solvolysis reaction of phenyl chlorodithioformate was reported.

Application

Phenyl chlorodithioformate was used in synthesis of phenyl arylsulfonyl-alkyl-dithiocarbamates. It was also used in synthesis of S-phenyl O-(4-nitrophenyl)dithiocarbonate.

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 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCM3577
MKCL4766
MKBN7724V
MKBL6757V
MKBG2723V

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The nucleofuge in the pyridinolysis of O-(4-nitrophenyl) S-aryl thio and dithiocarbonates.
Castro EA, et al.
Journal of Physical Organic Chemistry, 25(11), 994-994 (2012)
Kinetics and mechanism of the reactions of aryl chlorodithioformates with pyridines and secondary alicyclic amines.
Castro EA, et al.
Journal of Physical Organic Chemistry, 22(11), 1030-1037 (2009)
Synthesis of Phenyl Arylsulfonyl-alkyl-dithiocarbamates and Their Hydrolytic Reactivity in Hydroxide and Hydroperoxide Media.
Norberto F, et al.
European Journal of Organic Chemistry, 2005(21), 4710-4714 (2005)

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