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Merck

665266

Sigma-Aldrich

(+)-1,2-双[(2S,5S)-2,5-二甲基磷]苯

kanata purity

别名:

(2S,2′S,5S,5′S)-2,2′,5,5′-四甲基-1,1′-(邻亚苯基)二磷烷, (S,S)-Me-DUPHOS, (S,S)-甲基-DUPHOS

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About This Item

经验公式(希尔记法):
C18H28P2
分子量:
306.36
Beilstein:
4810602
MDL號碼:
分類程式碼代碼:
12352005
PubChem物質ID:
NACRES:
NA.22

品質等級

形狀

solid

mp

67-76 °C

官能基

phosphine

SMILES 字串

C[C@H]1CC[C@H](C)P1c2ccccc2P3[C@@H](C)CC[C@@H]3C

InChI

1S/C18H28P2/c1-13-9-10-14(2)19(13)17-7-5-6-8-18(17)20-15(3)11-12-16(20)4/h5-8,13-16H,9-12H2,1-4H3/t13-,14-,15-,16-/m0/s1

InChI 密鑰

AJNZWRKTWQLAJK-VGWMRTNUSA-N

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法律資訊

与 Kanata Chemical Technologies, Inc. 联合销售,仅供研究使用。这些化合物由 E.I. du Pont de Nemours and Company 授权制造和销售,此许可不包括利用这些化合物制备在制药领域销售的产品的权利。

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)


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分析证书(COA)

Lot/Batch Number

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商品

We are proud to offer new catalysts for hydrogenation through our collaboration with Kanata Chemical Technologies.

We are proud to offer new catalysts for hydrogenation through our collaboration with Kanata Chemical Technologies.

Asymmetric hydrogenation reactions represent the ideal process for the commercial manufacture of single-enantiomer compounds, because of the ease by which these robust procedures can be scaled up and because of the low levels of byproducts generated in these asymmetric hydrogenations.

Asymmetric hydrogenation reactions represent the ideal process for the commercial manufacture of single-enantiomer compounds, because of the ease by which these robust procedures can be scaled up and because of the low levels of byproducts generated in these asymmetric hydrogenations.

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