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化驗
97%
形狀
solid
光學活性
[α]20/D -57.0°, c = 1 in chloroform
mp
147-152 °C
SMILES 字串
CN(Cc1ccccc1)C(=O)[C@@H](NC(=S)Nc2cc(cc(c2)C(F)(F)F)C(F)(F)F)C(C)(C)C
InChI
1S/C23H25F6N3OS/c1-21(2,3)18(19(33)32(4)13-14-8-6-5-7-9-14)31-20(34)30-17-11-15(22(24,25)26)10-16(12-17)23(27,28)29/h5-12,18H,13H2,1-4H3,(H2,30,31,34)/t18-/m1/s1
InChI 密鑰
LTFFYVVCUVYZPE-GOSISDBHSA-N
一般說明
(S)-2-[[3,5-Bis(trifluoromethyl)phenyl]thioureido]-N-benzyl-N,3,3-trimethylbutanamide is a chiral thiourea organocatalyst developed by the Jacobsen′s group for asymmetric organic synthesis.
應用
催化包括 Mannich 反应在内的多种反应的多功能催化剂。
訊號詞
Warning
危險分類
Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 4 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
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
dust mask type N95 (US), Eyeshields, Gloves
Divergent Stereoinduction Mechanisms in Urea-Catalyzed Additions to Imines
Synlett, 1919-1919 (2003)
相关内容
Jacobsen's group have developed a range of chiral thioureas that are versatile, effective organocatalysts.
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