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Merck
CN

513210

(S)-(−)-2-甲基-2-丙烷亚磺酰胺

97%

别名:

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

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关于此项目

线性分子式:
(CH3)3CS(O)NH2
化学文摘社编号:
343338-28-3
分子量:
121.20
MDL编号:
MFCD05861480
UNSPSC代码:
12352111
PubChem化学物质编号:
24873681
NACRES:
NA.22

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质量水平

100

方案

97%

旋光性

[α]20/D −4.5°, c = 1 in chloroform

mp

97-101 °C (lit.)

储存温度

2-8°C

SMILES字符串

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

InChI

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

InChI key

CESUXLKAADQNTB-ZETCQYMHSA-N

相关类别

应用

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。

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
MKCX5785
MKCQ1917
MKCK8329
MKCC8950
MKCB1775V

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Synthesis and structure-activity relationships of novel benzofuran farnesyltransferase inhibitors.
Asoh K, et al.
Bioorganic & Medicinal Chemistry Letters, 19(6), 1753-1757 (2009)
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)
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
Jeffrey P McMahon et al.
Organic letters, 6(10), 1645-1647 (2004-05-07)
Addition of alkyl or aryl Grignard reagents to N-sulfinyl imines derived from 3- and 4-substituted cyclohexanones proceeds with good yields and with excellent diasteroselectivity. The selectivity of the reaction is controlled by the ring substituent rather than the sulfinyl group
Journal of the American Chemical Society, 119, 9913-9914 (1997)
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商品

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.

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Ellman Group – Professor Product Portal

Ellman group developed electron-rich phosphine ligands for C-H functionalization and tert-Butanesulfinamide for asymmetric amine synthesis.

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