Dibenzyl disulfide - CAS 150-60-7

Catalog:	BB010559
Product Name:	Dibenzyl disulfide
CAS:	150-60-7
Synonyms:	(benzyldisulfanyl)methylbenzene

Technical Data

Safety and Hazards

Patents

Literatures

Computed Properties

IUPAC Name:	(benzyldisulfanyl)methylbenzene
Description:	Originating from Petiveria alliacea L. This compound along with the other sulfur-containing compound found in this plant display antibacterial and antifungal activity.
Molecular Weight:	246.39
Molecular Formula:	C14H14S2
Canonical SMILES:	C1=CC=C(C=C1)CSSCC2=CC=CC=C2
InChI:	InChI=1S/C14H14S2/c1-3-7-13(8-4-1)11-15-16-12-14-9-5-2-6-10-14/h1-10H,11-12H2
InChI Key:	GVPWHKZIJBODOX-UHFFFAOYSA-N
Boiling Point:	270 °C (Decomposes)
Melting Point:	71 - 72 °C
Density:	1.3 g/cm³
Appearance:	Solid
MDL:	MFCD00004783
LogP:	4.76820

Publication Number	Title	Priority Date
CN-113244393-A	Titanium dioxide nanotube/molybdenum disulfide nanoflower compound and preparation method and application thereof	20210518
CN-113201083-A	Sulfur-doped C3N4Preparation method and application of poly (1, 4-diphenyl diacetylene)/polyaniline photocatalytic material	20210508
CN-113122353-A	Special oil for maintaining telescopic arm of crane and preparation method thereof	20210401
CN-112844369-A	Heavy oil slurry bed hydrogenation carbon-carried monoatomic molybdenum catalyst and preparation and application method thereof	20210301
CN-112844440-A	Heavy oil slurry bed hydrogenation carbon-supported molybdenum-cobalt diatomic catalyst and preparation method and application method thereof	20210301

PMID	Publication Date	Title	Journal
22311820	20120301	Simultaneous liquid-liquid extraction of dibenzyl disulfide, 2,6-di-tert-butyl-p-cresol, and 1,2,3-benzotriazole from power transformer oil prior to GC and HPLC determination	Journal of separation science
21977054	20120101	Natural products from ethnodirected studies: revisiting the ethnobiology of the zombie poison	Evidence-based complementary and alternative medicine : eCAM
20715797	20100909	Functional groups and sulfur K-edge XANES spectra: divalent sulfur and disulfides	The journal of physical chemistry. A
20042296	20100325	Acaricidal activity of extracts from Petiveria alliacea (Phytolaccaceae) against the cattle tick, Rhipicephalus (Boophilus) microplus (Acari: ixodidae)	Veterinary parasitology
19827080	20091123	A fragment-based approach to probing adenosine recognition sites by using dynamic combinatorial chemistry	Chembiochem : a European journal of chemical biology

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Related Functional Groups

Sulfur Compounds

[518012-62-9]
[2-[2-(2-Methoxyethoxy)ethoxy]ethoxy]p-toluenesulfonate
[6633-90-5]
1,4-Butanedithiol diacetate
[85-47-2]
1-Naphthalenesulfonic acid
[832739-73-8]
4-(3,5-Dichlorophenyl)pyrimidine-2-thiol
[6358-69-6]
8-Hydroxypyrene-1,3,6-trisulfonic acid trisodium salt
[843673-72-3]
(R)-4-(1-((tert-Butoxycarbonyl)amino)-2-hydroxyethyl)phenyl trifluoromethanesulfonate

GHS Hazard Statement:	H317 (100%): May cause an allergic skin reaction [Warning Sensitization, Skin]
Precautionary Statement:	P261, P264, P272, P280, P302+P352, P305+P351+P338, P321, P333+P313, P337+P313, P363, and P501
Signal Word:	Warning

Complexity:	150
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	246.05369279
Formal Charge:	0
Heavy Atom Count:	16
Hydrogen Bond Acceptor Count:	2
Hydrogen Bond Donor Count:	0
Isotope Atom Count:	0
Monoisotopic Mass:	246.05369279
Rotatable Bond Count:	5
Topological Polar Surface Area:	50.6 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	3.9