3,5-Bis(trifluoromethyl)benzene-1-sulfonyl chloride

Modify Date: 2025-08-25 12:49:04

3,5-Bis(trifluoromethyl)benzene-1-sulfonyl chloride structure	Common Name	3,5-Bis(trifluoromethyl)benzene-1-sulfonyl chloride
	CAS Number	39234-86-1	Molecular Weight	312.617
	Density	1.6±0.1 g/cm3	Boiling Point	248.3±40.0 °C at 760 mmHg
	Molecular Formula	C₈H₃ClF₆O₂S	Melting Point	34-38 °C(lit.)
	MSDS	Chinese USA	Flash Point	104.0±27.3 °C
	Symbol	GHS05	Signal Word	Danger

Name	3,5-bis(trifluoromethyl)benzenesulfonyl chloride
Synonym	More Synonyms

Density	1.6±0.1 g/cm3
Boiling Point	248.3±40.0 °C at 760 mmHg
Melting Point	34-38 °C(lit.)
Molecular Formula	C₈H₃ClF₆O₂S
Molecular Weight	312.617
Flash Point	104.0±27.3 °C
Exact Mass	311.944641
PSA	42.52000
LogP	4.07
Vapour Pressure	0.0±0.5 mmHg at 25°C
Index of Refraction	1.435
Storage condition	Refrigerator

MSDS(Chinese)

Symbol	GHS05
Signal Word	Danger
Hazard Statements	H314
Precautionary Statements	P280-P305 + P351 + P338-P310
Personal Protective Equipment	Eyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges
Hazard Codes	C:Corrosive;
Risk Phrases	R34
Safety Phrases	S26-S36-S36/37/39
RIDADR	UN 3261 8/PG 2
WGK Germany	3
Packaging Group	III
Hazard Class	8
HS Code	2904909090

3,5-Di(trifluor...

CAS#:328-74-5

3,5-Bis(trifluo...

CAS#:39234-86-1

Literature: Hoffman, Robert V.; Belfoure, Edward L. Journal of the American Chemical Society, 1982 , vol. 104, # 8 p. 2183 - 2189

Precursor 1
CAS#:328-74-5 3,5-Di(trifluor...
DownStream 3
CAS#:111711-53-6 1-[3,5-bis(trif... CAS#:130783-02-7 3,5-Bis(trifluo... CAS#:39213-22-4 3,5-bis(trifluo...

HS Code	2904909090
Summary	HS:2904909090 sulphonated, nitrated or nitrosated derivatives of hydrocarbons, whether or not halogenated VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

New library of aminosulfonyl-tagged Hoveyda-Grubbs type complexes: Synthesis, kinetic studies and activity in olefin metathesis transformations.

Beilstein J. Org. Chem. 6 , 1159-66, (2010)

Seven novel Hoveyda-Grubbs precatalysts bearing an aminosulfonyl function are reported. Kinetic studies indicate an activity enhancement compared to Hoveyda's precatalyst. A selection of these catalys...

Highly enantioselective catalytic thiolysis of prochiral cyclic dicarboxylic anhydrides utilizing a bifunctional chiral sulfonamide.

Angew. Chem. Int. Ed. Engl. 44(36) , 5838-41, (2005)

Versatile chiral reagent for the highly enantioselective synthesis of either anti or syn ester aldols. Corey EJ and Kim SS.

J. Am. Chem. Soc. 112(12) , 4976-4977, (1990)

3,5-bis(trifluoromethyl)benzene sulfonyl chloride

EINECS 254-371-0

3,5-Bis(trifluoromethyl)benzene-1-sulfonyl chloride

MFCD00014725

WSGR CXFFF EXFFF

Benzenesulfonyl chloride, 3,5-bis(trifluoromethyl)-

3,5-(bistrifluoromethyl)phenylsulfonyl chloride

3,5-Bis(trifluoromethyl)benzenesulphonyl chloride