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ETHYL 1,3-DITHIOLANE-2-CARBOXYLATE

ETHYL 1,3-DITHIOLANE-2-CARBOXYLATE Structure
CAS No.
20461-99-8
Chemical Name:
ETHYL 1,3-DITHIOLANE-2-CARBOXYLATE
Synonyms
2-Carboethoxydithiolane;2-Carboethoxy-1,3-dithiolane;2-Ethoxycarbonyl-1,3-dithiolane;Ethyl 1,3-Ditholane-2-carboxylate;ETHYL 1,3-DITHIOLANE-2-CARBOXYLATE;ETHYL GLYOXYLATE ETHYLENE THIOACETAL;Ethyl 1,3-dithiolane-2-carboxylate,99%;Ethyl 1,3-dithiolane-2-carboxylate, 98+%;Ethyl 1,3-dithiolane-2-carboxylate, GC 99%;Ethyl 1,3-dithiolane-2-carboxylate, 99% 5ML
CBNumber:
CB2105967
Molecular Formula:
C6H10O2S2
Molecular Weight:
178.27
MOL File:
20461-99-8.mol
Modify Date:
2023/6/8 17:06:36

ETHYL 1,3-DITHIOLANE-2-CARBOXYLATE Properties

Boiling point 85 °C/0.1 mmHg (lit.)
Density 1.249 g/mL at 25 °C (lit.)
refractive index n20/D 1.539(lit.)
Flash point >230 °F
storage temp. 2-8°C
form Liquid
color Clear light yellow
Specific Gravity 1.249
BRN 118157
CAS DataBase Reference 20461-99-8(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Safety Statements  23-24/25
RIDADR  3334
WGK Germany  3
8-9
HS Code  29349990
NFPA 704
1
0 0

ETHYL 1,3-DITHIOLANE-2-CARBOXYLATE price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemicals (India) D2105 Ethyl 1,3-Dithiolane-2-carboxylate min. 97.0 % 20461-99-8 5G ₹5400 2022-05-26 Buy
Product number Packaging Price Buy
D2105 5G ₹5400 Buy

ETHYL 1,3-DITHIOLANE-2-CARBOXYLATE Chemical Properties,Uses,Production

Chemical Properties

clear light yellow liquid

General Description

Ethyl 1,3-dithiolane-2-carboxylate is an α-keto acid equivalent. It participates in the conjugate additions to enones. It is a bulky equivalent of acetate undergoing syn-selective aldol reactions. Anion derived from ethyl 1,3-dithiolane-2-carboxylate participates as nucleophile during the total synthesis of the corynanthe alkaloid dihydrocorynantheol and the formal syntheses of the indole alkaloids tacamonine, rhynchophylline and hirsutine. It also participates in the conjugate addition of enolates to phenylglycinol-derived α,β-unsaturated δ-lactams.

Purification Methods

Dissolve the ester in CHCl3, wash it with aqueous K2CO3, twice with H2O, dry it over MgSO4, filter, evaporate and distil the residue in vacuo. [Hermann et al Tetrahedron Lett 2599 1973, Corey & Erickson J Org Chem 36 3553 1971]. [Beilstein 19/7 V 225.]

ETHYL 1,3-DITHIOLANE-2-CARBOXYLATE Preparation Products And Raw materials

Global( 70)Suppliers
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TCI Chemicals (India) Pvt. Ltd. 1800 425 7889 New Delhi, India 6778 58 Inquiry
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Aladdin Scientific +1-+1(833)-552-7181 United States 52927 58 Inquiry
Amadis Chemical Company Limited 571-89925085 China 131980 58 Inquiry
ETHYL 1,3-DITHIOLANE-2-CARBOXYLATE ETHYL GLYOXYLATE ETHYLENE THIOACETAL GLYOXYLIC ACID ETHYL ESTER ETHYLENE MERCAPTAL 2-Carboethoxy-1,3-dithiolane~1,3-Dithiolane-2-carboxylicacidethylester~2-Ethoxycarbonyl-1,3-dithiolane~Ethylglyoxyla 1,3-DITHIOLANE-2-CARBOXYLIC ACID ETHYL ESTER 2-Carboethoxy-1,3-dithiolane 2-Carboethoxydithiolane Ethyl 1,3-dithiolane-2-carboxylate, GC 99% 1,3-DITHIOLANE-2-CARBOXYLIC ACID ETHYL ESTER 95+% Ethyl 1,3-dithiolane-2-carboxylate, 98+% Ethyl 1,3-dithiolane-2-carboxylate,99% 2-Ethoxycarbonyl-1,3-dithiolane Ethyl Glyoxylate Dimethylene Dithioacetal Ethyl 1,3-dithiolane-2-carboxylate, 99% 5ML Ethyl 1,3-Ditholane-2-carboxylate 20461-99-8 C6H10O2S2 Sulfur Compounds (for Synthesis) Building Blocks Others S-Containing Heterocyclic Building Blocks Sulfur Compounds (for Synthesis) Synthetic Organic Chemistry Heterocyclic Compounds