(4S)-4-t-Butyl-1,2,3-oxathiazolidine-2,2-dioxide-3-carboxylic acid t-butyl ester, Min. 97%

Base Information

Chemical Name:(4S)-4-t-Butyl-1,2,3-oxathiazolidine-2,2-dioxide-3-carboxylic acid t-butyl ester, Min. 97%
CAS No.:1206227-45-3
Molecular Formula:C₁₁H₂₁NO₅S
Molecular Weight:279.357
Hs Code.:
Mol file:1206227-45-3.mol

Synonyms:(4S)-4-tert-butyl-1,2,3-oxathiazolidine-3-carboxylic acid 1,1-dimethylethyl ester 2,2-dioxide

Suppliers and Price of (4S)-4-t-Butyl-1,2,3-oxathiazolidine-2,2-dioxide-3-carboxylic acid t-butyl ester, Min. 97%

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Strem Chemicals
(4S)-4-t-Butyl-1,2,3-oxathiazolidine-2,2-dioxide-3-carboxylic acid t-butyl ester, min. 97%
1g
$ 214.00

Strem Chemicals
(4S)-4-t-Butyl-1,2,3-oxathiazolidine-2,2-dioxide-3-carboxylic acid t-butyl ester, min. 97%
250mg
$ 72.00

Crysdot
(S)-tert-Butyl4-(tert-butyl)-1,2,3-oxathiazolidine-3-carboxylate2,2-dioxide 95+%
1g
$ 424.00

ACHEMBLOCK
(S)-3-Boc-4-(tert-butyl)-1,2,3-oxathiazolidine2,2-dioxide 95%
250MG
$ 270.00

Total 8 raw suppliers

Chemical Property of (4S)-4-t-Butyl-1,2,3-oxathiazolidine-2,2-dioxide-3-carboxylic acid t-butyl ester, Min. 97%

Chemical Property:

Melting Point:115.0-155.5 °C(Solv: dichloromethane (75-09-2); hexane (110-54-3))
Boiling Point:329.6±25.0 °C(Predicted)
PKA:-13.53±0.40(Predicted)
Density:1.210±0.06 g/cm3(Predicted)
Sensitive.:air sensitive

Purity/Quality:

98% ^*data from raw suppliers

(4S)-4-t-Butyl-1,2,3-oxathiazolidine-2,2-dioxide-3-carboxylic acid t-butyl ester, min. 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of (4S)-4-t-Butyl-1,2,3-oxathiazolidine-2,2-dioxide-3-carboxylic acid t-butyl ester, Min. 97%

There total 5 articles about (4S)-4-t-Butyl-1,2,3-oxathiazolidine-2,2-dioxide-3-carboxylic acid t-butyl ester, Min. 97% which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 79.0%

: 1206227-45-3
(4S)-4-tert-butyl-1,2,3-oxathiazolidine-3-carboxylic acid 1,1-dimethylethyl ester 2,2-dioxide

Guidance literature:: With sulfuryl dichloride; N-ethyl-N,N-diisopropylamine; In 1,2-dichloro-ethane; at -10 ℃; for 1h; Inert atmosphere;

Reference yield:

: C₁₁H₂₁NO₄S

: 1206227-45-3
(4S)-4-tert-butyl-1,2,3-oxathiazolidine-3-carboxylic acid 1,1-dimethylethyl ester 2,2-dioxide

Guidance literature:: With sodium periodate; ruthenium(III) chloride trihydrate; In water; acetonitrile; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1021/jo902302c

Reference yield:

: 112245-13-3
(S)-tert-leucinol

: 1206227-45-3
(4S)-4-tert-butyl-1,2,3-oxathiazolidine-3-carboxylic acid 1,1-dimethylethyl ester 2,2-dioxide

Guidance literature:: Multi-step reaction with 3 steps

1: sodium carbonate / tetrahydrofuran; water / Cooling with ice

2: thionyl chloride; pyridine / acetonitrile / 3 h / -40 - 20 °C / Inert atmosphere

3: rhodium(III) chloride hydrate; sodium periodate / water; acetonitrile / 1 h / 0 - 20 °C

With pyridine; sodium periodate; thionyl chloride; rhodium(III) chloride hydrate; sodium carbonate; In tetrahydrofuran; water; acetonitrile;
DOI:10.1002/adsc.201500110