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Merck

649317

Sigma-Aldrich

(R)-(+)-2-甲基-CBS-噁唑硼烷

别名:

(R)-1-甲基-3,3-二苯基六氢吡咯并[1,2-c][1,3,2]恶唑硼啉, (R)-3,3-二苯基-1-甲基吡咯烷[1,2-c]-1,3,2-恶唑硼啉, (R)-Me-Corey-Bakshi-Shibata催化剂

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About This Item

经验公式(希尔记法):
C18H20BNO
分子量:
277.17
MDL號碼:
分類程式碼代碼:
12352005
PubChem物質ID:
NACRES:
NA.22

化驗

≥90%

品質等級

形狀

solid

mp

85-95 °C (lit.)

SMILES 字串

CB1OC(C2CCCN12)(c3ccccc3)c4ccccc4

InChI

1S/C18H20BNO/c1-19-20-14-8-13-17(20)18(21-19,15-9-4-2-5-10-15)16-11-6-3-7-12-16/h2-7,9-12,17H,8,13-14H2,1H3/t17-/m1/s1

InChI 密鑰

VMKAFJQFKBASMU-QGZVFWFLSA-N

應用

CBS(Corey-Bakshi-Shibata)恶唑硼烷催化剂已被用于前手性酮的不对称还原。其它应用包括对映选择性合成α-羟基酸、α- 氨基酸、 C2对称二茂铁基二醇和炔丙醇。

象形圖

CorrosionExclamation mark

訊號詞

Danger

危險聲明

危險分類

Acute Tox. 4 Oral - Eye Dam. 1

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)


分析证书(COA)

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在文件库中查找您最近购买产品的文档。

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Sing, V. K.
Synthesis, 605-605 (1992)
Asymmetric Reduction. A Convenient Method for the Reduction of Alkynyl Ketones.
Kathlyn A. Parker et al.
The Journal of organic chemistry, 61(9), 3214-3217 (1996-05-03)
Angewandte Chemie (International Edition in English), 37, 1986-1986 (1998)
Current Science, 78, 1314-1317 (2000)
E.J. Corey et al.
Tetrahedron Letters, 31, 611-611 (1990)

商品

we are pleased to offer both enatiomers of 2-methyl-CBS-oxazaborolidine as a dry reagent, in addition to our current offerings as a 1M solution in toluene.

Learn about the applications of chiral oxazaborolidinium ions (COBIs) as Lewis acid catalysts in different asymmetric reactions such as cyclopropanation, epoxidation, and radical reactions along with details of their catalytic action.

Learn about the applications of chiral oxazaborolidinium ions (COBIs) as Lewis acid catalysts in different asymmetric reactions such as cyclopropanation, epoxidation, and radical reactions along with details of their catalytic action.

Learn about the applications of chiral oxazaborolidinium ions (COBIs) as Lewis acid catalysts in different asymmetric reactions such as cyclopropanation, epoxidation, and radical reactions along with details of their catalytic action.

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