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Ethyl 1,3-dithiane-2-carboxylate

Ethyl 1,3-dithiane-2-carboxylate Structure
CAS No.
20462-00-4
Chemical Name:
Ethyl 1,3-dithiane-2-carboxylate
Synonyms
Carboethoxy-1,3-dithiane;2-Carboethoxy-1,3-dithiane;2-Ethoxycarbonyl-1,3-dithiane;ETHYL 1,3-DITHIANE-2-CARBOXYLATE;Ethyl1,3-Dithiane-2-carboxylate>Ethyl 1,3-dithiane-2-carboxylate, 98+%;ETHYL-1 3-DITHIANE-2-CARBOXYLATE 99% (&;ETHYL 1,3-DITHIANE-2-CARBOXYLATE FOR SYN;2-(2-phenylimino-3-thiazolidinyl)ethanol;m-Dithiane-2-carboxylic acid, ethyl ester
CBNumber:
CB6490333
Molecular Formula:
C7H12O2S2
Molecular Weight:
192.3
MOL File:
20462-00-4.mol
MSDS File:
SDS
Modify Date:
2023/10/31 10:56:06

Ethyl 1,3-dithiane-2-carboxylate Properties

Melting point 19-21°C
Boiling point 75-77 °C/0.2 mmHg (lit.)
Density 1.22 g/mL at 25 °C (lit.)
refractive index n20/D 1.539(lit.)
Flash point 130 °F
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form clear liquid
color Colorless to Light yellow to Light orange
Water Solubility Slightly miscible with water.
BRN 1424352
InChI InChI=1S/C7H12O2S2/c1-2-9-6(8)7-10-4-3-5-11-7/h7H,2-5H2,1H3
InChIKey ANEDZEVDORCLPM-UHFFFAOYSA-N
SMILES S1CCCSC1C(OCC)=O
CAS DataBase Reference 20462-00-4(CAS DataBase Reference)
NIST Chemistry Reference Ethyl 1,3-dithiane-2-carboxylate(20462-00-4)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS02
Signal word  Warning
Hazard statements  H226
Precautionary statements  P241-P280a-P501a-P210-P233-P240-P241+P242+P243-P280-P303+P361+P353-P403+P235-P501
Risk Statements  10
Safety Statements  26-36/37/39-45
RIDADR  UN 3272 3/PG 3
WGK Germany  3
9-13
HazardClass  3
PackingGroup  III
HS Code  29349990
NFPA 704
2
1 0

Ethyl 1,3-dithiane-2-carboxylate price More Price(5)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 43749 Ethyl 1,3-dithiane-2-carboxylate technical, ≥90% (GC) 20462-00-4 5ML ₹14710 2022-06-14 Buy
TCI Chemicals (India) D1648 Ethyl 1,3-Dithiane-2-carboxylate min. 98.0 % 20462-00-4 1G ₹2300 2022-05-26 Buy
ALFA India ALF-L00663-14 Ethyl 1,3-dithiane-2-carboxylate, 98+% 20462-00-4 25g ₹32253 2022-05-26 Buy
TCI Chemicals (India) D1648 Ethyl 1,3-Dithiane-2-carboxylate min. 98.0 % 20462-00-4 5G ₹8800 2022-05-26 Buy
ALFA India ALF-L00663-06 Ethyl 1,3-dithiane-2-carboxylate, 98+% 20462-00-4 5g ₹5805 2022-05-26 Buy
Product number Packaging Price Buy
43749 5ML ₹14710 Buy
D1648 1G ₹2300 Buy
ALF-L00663-14 25g ₹32253 Buy
D1648 5G ₹8800 Buy
ALF-L00663-06 5g ₹5805 Buy

Ethyl 1,3-dithiane-2-carboxylate Chemical Properties,Uses,Production

Chemical Properties

clear yellowish liquid

Uses

Ethyl 1,3-dithiane-2-carboxylate is used in syn-selective aldol reactions. It undergoes asymmetric oxidation to give trans bis-sulfoxide. It is used to generate carbanon, which finds application in the preparation of alfa- keto esters.

Preparation

To a solution of BF3. Et2O (57.5 mL, 0.454 mmol) in CHC13 (180 mL) heated at reflux was added dropwise, over a 1h period, a solution of 1,3-propanedithiol (22.7 mL, 0.227 mmol), followed by ethyl diethoxyacetate (40 g, 0.227 mmol) in CHCl3 (40 mL). The resulting mixture was heated for 30 minutes, and then cooled to rt. The cooled solution was washed 2 times with water, once with saturated aqueous NaHC03, and then re-washed with water. The combined organic phases were dried over MgS04, then evaporated to give 41 g (94%) of Ethyl 1,3-dithiane-2-carboxylate as a yellow oi. Yield: 94%

Application

Ethyl 1,3-dithiane-2-carboxylate is a synthetic compound that is used in the synthesis of organic compounds . It is used in asymmetric synthesis to produce chiral products from achiral starting materials. The desulfurization reaction of ethyl 1,3-dithiane-2-carboxylate produces a mixture of the two possible stereoisomers of the product. This mixture can be separated by phase chromatography and then hydrolyzed to give the desired product. In dyslipidemia, ethyl 1,3-dithiane-2-carboxylate inhibits the activity of hepatic lipase and acidolysis. This inhibition leads to an increase in serum triglycerides and cholesterol levels. This compound also has been shown to have antiplatelet properties when administered orally or intravenously to rats without affecting platelet aggregation rates.

General Description

Ethyl 1,3-dithiane-2-carboxylate is an α-keto acid equivalent and bulky equivalent of acetate. It participates in syn-selective aldol reactions. It can be prepared from the reaction of ethyl diethoxyacetate and 1,3-propanedithiol in the presence of BF3/Et2O. Asymmetric oxidation of ethyl 1,3-dithiane-2-carboxylate by Modena protocol has been reported to afford trans bis-sulfoxide in 60% yield. Carbanion from ethyl 1,3-dithiane-2-carboxylate may be employed for the preparation of α-keto esters.

Purification Methods

Dissolve the ester in CHCl3, wash with aqueous K2CO3, twice with H2O, dry over MgSO4, filter, evaporate and distil the residue. [Eliel & Hartman J Org Chem 37 505 1972, Seebach Synthesis 1 17 1969, Beilstein 19/7 V 227.]

Ethyl 1,3-dithiane-2-carboxylate Preparation Products And Raw materials

Global( 121)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
CHEMSWORTH +91-261-2397244 New Delhi, India 6707 30 Inquiry
TCI Chemicals (India) Pvt. Ltd. 1800 425 7889 New Delhi, India 6778 58 Inquiry
Alfa Aesar 1 800 209 7001 Maharashtra, India 6913 58 Inquiry
Huida Pharmaceutical Technology (Shanghai) Co., Ltd. +8613601750004 China 439 58 Inquiry
Capot Chemical Co.,Ltd. 571-85586718 +8613336195806 China 29798 60 Inquiry
Shanghai Daken Advanced Materials Co.,Ltd +86-371-66670886 China 16220 58 Inquiry
ATK CHEMICAL COMPANY LIMITED +undefined-21-51877795 China 32760 60 Inquiry
CONIER CHEM AND PHARMA LIMITED +8618523575427 China 49391 58 Inquiry
career henan chemical co +86-0371-86658258 +8613203830695 China 29826 58 Inquiry
Neostar United (Changzhou) Industrial Co., Ltd. +86-519-519-85557386 China 12210 58 Inquiry
ETHYL-1 3-DITHIANE-2-CARBOXYLATE 99% (& Ethyl 1,3-dithiane-2-carboxylate, 98+% 2-Ethoxycarbonyl-1,3-dithiane Ethyl Glyoxylate Trimethylene Dithioacetal ETHYL 1,3-DITHIANE-2-CARBOXYLATE FOR SYN m-Dithiane-2-carboxylic acid, ethyl ester 2-Carboethoxy-1,3-dithiane Carboethoxy-1,3-dithiane GLYOXYLIC ACID ETHYL ESTER TRIMETHYLENEMERCAPTAL ETHYL 1,3-DITHIANE-2-CARBOXYLATE 1,3-DITHIANE-2-CARBOXYLIC ACID ETHYL ESTER 2-(2-phenylimino-3-thiazolidinyl)ethanol Ethyl1,3-Dithiane-2-carboxylate> 20462-00-4 C7H12O2S2 Others Sulfur Compounds (for Synthesis) Building Blocks Heterocyclic Building Blocks S-Containing Heterocyclic Compounds Sulfur Compounds (for Synthesis) Synthetic Organic Chemistry Sulfur compounds