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Ethyl 1,3-dithiane-2-carboxylate

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
MDL Number:
MFCD00006657
MOL File:
20462-00-4.mol
MSDS File:
SDS
Last updated: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)
FDA UNII DRA87T4JKT
NIST Chemistry Reference Ethyl 1,3-dithiane-2-carboxylate(20462-00-4)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
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(17)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 43749 Ethyl 1,3-dithiane-2-carboxylate technical, ≥90% (GC) 20462-00-4 5ml $296 2024-03-01 Buy
TCI Chemical D1648 Ethyl 1,3-Dithiane-2-carboxylate >98.0%(GC) 20462-00-4 1g $84 2024-03-01 Buy
TCI Chemical D1648 Ethyl 1,3-Dithiane-2-carboxylate >98.0%(GC) 20462-00-4 5g $231 2024-03-01 Buy
Alfa Aesar L00663 Ethyl 1,3-dithiane-2-carboxylate, 98+% 20462-00-4 5g $93.4 2024-03-01 Buy
Alfa Aesar L00663 Ethyl 1,3-dithiane-2-carboxylate, 98+% 20462-00-4 25g $372 2024-03-01 Buy
Product number Packaging Price Buy
43749 5ml $296 Buy
D1648 1g $84 Buy
D1648 5g $231 Buy
L00663 5g $93.4 Buy
L00663 25g $372 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.

Synthesis Reference(s)

Synthetic Communications, 11, p. 343, 1981 DOI: 10.1080/00397918108063615

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.]

109-80-8
6065-82-3
20462-00-4
Synthesis of Ethyl 1,3-dithiane-2-carboxylate from 1,3-Dimercaptopropane and Ethyl diethoxyacetate

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

Global( 120)Suppliers
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Huida Pharmaceutical Technology (Shanghai) Co., Ltd.
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0551-65418671 sales@tnjchem.com China 34572 58

View Lastest Price from Ethyl 1,3-dithiane-2-carboxylate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Ethyl 1,3-dithiane-2-carboxylate pictures 2023-12-04 Ethyl 1,3-dithiane-2-carboxylate
20462-00-4
US $0.00-0.00 / kg 0.1kg 98% 100kg Huida Pharmaceutical Technology (Shanghai) Co., Ltd.
Ethyl 1,3-dithiane-2-carboxylate pictures 2023-12-04 Ethyl 1,3-dithiane-2-carboxylate
20462-00-4
US $0.00-0.00 / kg 0.1kg 98% 100kg Huida Pharmaceutical Technology (Shanghai) Co., Ltd.
Ethyl 1,3-dithiane-2-carboxylate pictures 2022-09-30 Ethyl 1,3-dithiane-2-carboxylate
20462-00-4
US $0.00-0.00 / g 10g 98% 10kg Zhengzhou Gecko Scientific Inc.
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