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Merck
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536652

Sigma-Aldrich

(S)-(-)-2-(Boc-氨基)-1,4-丁二醇

97%

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About This Item

線性公式:
HOCH2CH2CH[NHCO2C(CH3)3]CH2OH
CAS號碼:
分子量::
205.25
MDL號碼:
分類程式碼代碼:
12352108
PubChem物質ID:
NACRES:
NA.22

化驗

97%

光學活性

[α]20/D −8°, c = 1 in chloroform

mp

65-69 °C (lit.)

SMILES 字串

CC(C)(C)OC(=O)N[C@H](CO)CCO

InChI

1S/C9H19NO4/c1-9(2,3)14-8(13)10-7(6-12)4-5-11/h7,11-12H,4-6H2,1-3H3,(H,10,13)/t7-/m0/s1

InChI 密鑰

KLRRFBSWOIUAHZ-ZETCQYMHSA-N

應用

(S)-(−)-2-(Boc-amino)-1,4-butanediol can be used as a reactant to synthesize:
  • Thiourea-based organocatalysts for asymmetric Michael addition reactions of nitroalkenes to α-nitrocyclohexanone.
  • Bis-copper (II) complex based catalysts for enantioselective Michael reactions.

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)


分析證明 (COA)

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Asymmetric Michael additions of α-nitrocyclohexanone to aryl nitroalkenes catalyzed by natural amino acid-derived bifunctional thioureas
Jo?rres M, et al.
Organic Letters, 14(17), 4518-4521 (2012)
Copper (II) in organic synthesis. XI. Evaluation of the ligand architecture on the efficiency of a copper (II) catalyst for enantioselective Michael reactions
Desimoni G, et al.
Tetrahedron, 51(14), 4131-4144 (1995)

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