All Photos(1)
Synonym(s):
Ethanethiol sodium salt, Ethyl mercaptan sodium salt
Linear Formula:
CH3CH2SNa
CAS Number:
Molecular Weight:
84.12
Beilstein:
3593647
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
grade
technical
Quality Level
Assay
~90% (RT)
form
crystals
SMILES string
CCS[Na]
InChI
1S/C2H6S.Na/c1-2-3;/h3H,2H2,1H3;/q;+1/p-1
InChI key
QJDUDPQVDAASMV-UHFFFAOYSA-M
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Related Categories
Application
Sodium ethanethiolate is a reagent generally used to synthesize various thioethers. It can be employed as a ligand in the preparation of organometallic complexes. It is also used in the synthesis of thiolated amino-alcohols.
Other Notes
Alkanethiolates are efficient reagents for SN2 dealkylation of esters and aryl ethers
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Supplementary Hazards
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Novel thiolated amino-alcohols as chiral ligands for copper-catalyzed asymmetric nitro-aldol reactions.
Mansawat, Woraluk et al.
Tetrahedron Letters, 48(24), 4235-4238 (2007)
G.I. Feutrill et al.
Tetrahedron Letters, 1327-1327 (1970)
P.A. Bartlett et al.
Tetrahedron Letters, 4459-4459 (1970)
Kojyl thioether derivatives having both tyrosinase inhibitory and anti-inflammatory properties.
Rho, Ho Sik et al.
Bioorganic & Medicinal Chemistry Letters, 20(22), 6569-6571 (2010)
Mononuclear Ni (III) Complexes [NiIII (L)(P (C6H3-3-SiMe3-2-S) 3)] 0/1-(L= Thiolate, Selenolate, CH2CN, Cl, PPh3): Relevance to the Nickel Site of [NiFe] Hydrogenases.
Lee, Chien-Ming et al.
Inorganic Chemistry, 45(26), 10895-10904 (2006)
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