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518379

Sigma-Aldrich

Butylboronic acid N,N,N′,N′-tetramethyl-L-tartaric acid diamide ester

Synonym(s):

(4R,5R)-2-Butyl-N,N,N′,N′-tetramethyl-1,3,2-dioxaborolane-4,5-dicarboxamide

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About This Item

Empirical Formula (Hill Notation):
C12H23BN2O4
CAS Number:
Molecular Weight:
270.13
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

optical activity

[α]20/D -105°, c = 1.7% in chloroform

refractive index

n20/D 1.478 (lit.)

bp

178-179 °C (lit.)

density

1.072 g/mL at 25 °C (lit.)

functional group

amide

SMILES string

CCCCB1O[C@H]([C@@H](O1)C(=O)N(C)C)C(=O)N(C)C

InChI

1S/C12H23BN2O4/c1-6-7-8-13-18-9(11(16)14(2)3)10(19-13)12(17)15(4)5/h9-10H,6-8H2,1-5H3/t9-,10-/m1/s1

InChI key

AFQWQRBBIZKYTE-NXEZZACHSA-N

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Application

Butylboronic acid N,N,N′,N′-tetramethyl-L-tartaric acid diamide ester can be used as a cyclopropanation ligand in one of the key steps for the total synthesis of:
  • (+)-Frondosin, a natural product from marine sponges.
  • Marine cyanobacterium natural products: coibacins A and B.

Reactant for:
Preparation of biologically and pharmacologically active molecules

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Coibacins A and B: Total synthesis and stereochemical revision
Carneiro VMT, et al.
The Journal of Organic Chemistry, 79(2), 630-642 (2014)
Total synthesis of (+)-frondosin A. Application of the Ru-catalyzed [5+ 2] cycloaddition.
Trost, Barry M and Hu, Yimin and Horne, Daniel B
Journal of the American Chemical Society, 129(38), 11781-11790 (2007)

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