跳轉至內容
Merck
全部照片(2)

Key Documents

View All Documentation

513210

Sigma-Aldrich

(S)-(−)-2-甲基-2-丙烷亚磺酰胺

97%

同義詞:

(S)-(-)-tert-Butanesulfinamide, (S)-(-)-tert-Butyl sulfinamide, (S)-2-Methyl-2-propanesulfinamide, (S)-tert-Butanesulfinamide, (S)-tert-Butylsulfinamide

登入查看組織和合約定價
全部照片(2)

About This Item

線性公式:
(CH3)3CS(O)NH2
CAS號碼:
343338-28-3
分子量：:
121.20
MDL號碼:
MFCD05861480
分類程式碼代碼:
12352111
PubChem物質ID:
24873681
NACRES:
NA.22

化驗

97%

光學活性

[α]20/D −4.5°, c = 1 in chloroform

mp

97-101 °C (lit.)

儲存溫度

2-8°C

SMILES 字串

CC(C)(C)S(N)=O

InChI

1S/C4H11NOS/c1-4(2,3)7(5)6/h5H2,1-3H3/t7-/m0/s1

InChI 密鑰

CESUXLKAADQNTB-ZETCQYMHSA-N

相關類別

應用

叔丁基亚磺酰胺
(S)-(-)-2-甲基-2-丙亚磺酰胺可用于开发基于苯并呋喃的法呢基转移酶抑制剂作为抗癌剂。 它也可用于制备 (20E)-N-[叔丁基-(S)-亚磺酰基]-3β-(叔丁基二甲基甲硅烷氧基)-孕-5-烯-20-亚胺，它是用于制备雄激素受体拮抗剂的中间体。
作为手性助剂用于三氟乙胺的不对称制备，方法是将三氟乙醛转化为手性亚胺，然后用芳基锂处理和酸性甲醇分解。
用于合成手性胺的有效试剂。
通过与醛和酮缩合，易于转化为P,N-亚磺酰亚胺配体，它可以用于铱催化的烯烃不对称氢化。

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)

從最近期的版本中選擇一個：

分析證明 (COA)

Lot/Batch Number
MKCQ1917
MKCK8329
MKCC8950
MKCB1775V
MKBZ2676V

未看到正確版本？

如果您需要一個特定的版本，您可以透過批號來尋找特定憑證。

搜尋 COA

已經擁有該產品？

您可以在文件庫中找到最近購買的產品相關文件。

存取文件庫

Vouy Linh Truong et al.
Organic letters, 9(4), 683-685 (2007-01-30)
Condensation of N-tert-butanesulfinamide (S)-1 with trifluoroacetaldehyde hydrate 2a afforded 2-methyl-N-(2,2,2-trifluoroethylidene)propane-2-sulfinamide 3. Without isolation and purification, imine 3 was added to various aryllithium reagents to give highly diastereomerically enriched adducts 5a-g. Acidic methanolysis of 5a-g provided the desired 1-aryl-2,2,2-trifluoroethylamine hydrochloride compounds
20-Aminosteroids as a novel class of selective and complete androgen receptor antagonists and inhibitors of prostate cancer cell growth.
Fousteris MA, et al.
Bioorganic & Medicinal Chemistry Letters, 18(19), 6960-6969 (2010)
Synthesis and structure-activity relationships of novel benzofuran farnesyltransferase inhibitors.
Asoh K, et al.
Bioorganic & Medicinal Chemistry Letters, 19(6), 1753-1757 (2009)
Organic Letters, 69, 1800-1800 (2004)
Jonathan A Ellman et al.
Accounts of chemical research, 35(11), 984-995 (2002-11-20)
N-tert-Butanesulfinyl aldimines 3 and ketimines 4 are exceedingly versatile intermediates for the asymmetric synthesis of amines. The N-tert-butanesulfinyl imines are prepared in high yields by condensing enantiomerically pure tert-butanesulfinamide 1, which is readily available in either configuration, with a wide
查看所有相關論文

文章

Ellman's Sulfinamides

Ellman's sulfinamide is available in both enantiomeric and racemic forms for your research. This versatile and useful auxiliary has found extensive use both in academics and industry.

Ellman's Sulfinamides

Ellman's sulfinamide is available in both enantiomeric and racemic forms for your research. This versatile and useful auxiliary has found extensive use both in academics and industry.

我們的科學家團隊在所有研究領域都有豐富的經驗，包括生命科學、材料科學、化學合成、色譜、分析等.

聯絡技術服務