tris(methylthio)methane

Modify Date: 2025-08-26 10:38:10

tris(methylthio)methane Structure
tris(methylthio)methane structure
Common Name tris(methylthio)methane
CAS Number 5418-86-0 Molecular Weight 154.31700
Density 1.16 g/mL at 25ºC(lit.) Boiling Point 102ºC15 mm Hg(lit.)
Molecular Formula C4H10S3 Melting Point 16ºC(lit.)
MSDS Chinese USA Flash Point 204 °F
Symbol GHS07
GHS07
Signal Word Warning

 Names

Name tris(methylsulfanyl)methane
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.16 g/mL at 25ºC(lit.)
Boiling Point 102ºC15 mm Hg(lit.)
Melting Point 16ºC(lit.)
Molecular Formula C4H10S3
Molecular Weight 154.31700
Flash Point 204 °F
Exact Mass 153.99400
PSA 75.90000
LogP 2.35900
Index of Refraction n20/D 1.577(lit.)

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305 + P351 + P338
Personal Protective Equipment Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
Hazard Codes Xi: Irritant;
Risk Phrases R36/37/38
Safety Phrases 26-36
RIDADR UN 2810 6
WGK Germany 3
HS Code 2930909090

 Synthetic Route

 Customs

HS Code 2930909090
Summary 2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Articles3

More Articles
Catalytic enantioselective synthesis of naturally occurring butenolides via hetero-allylic alkylation and ring closing metathesis.

Org. Lett. 13(5) , 948-51, (2011)

An efficient catalytic asymmetric synthesis of chiral γ-butenolides was developed based on the hetero-allylic asymmetric alkylation (h-AAA) in combination with ring closing metathesis (RCM). The synth...

Research on L-nucleosides. Synthesis and biological evaluation of a series of L- and D-2',3'-dideoxy-3'-[tris(methylthio)methyl]-beta-pentofuranosyl nucleosides.

Bioorg. Med. Chem. 11(3) , 357-66, (2003)

Novel nucleoside analogues of both D and L enantiomeric series were prepared by coupling reaction between a 2',3'-dideoxy-3'-modified furanose moiety and four different nucleobases. Though in all case...

From ketones, aldehydes or alkyl halides to terminal 1, 1-difluoroolefins using BrF3. Hagooly A and Rozen S.

J. Fluor. Chem. 126(8) , 1239-45, (2005)

 Synonyms

Methyl orthotrithioformate
Trithiomethoxymethane
Trimethyl trithioorthoformate
Orthoformic acid,trithio-,trimethyl ester
MFCD00009851
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