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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

Quality Level

refractive index

n20/D 1.478 (lit.)

bp

178-179 °C (lit.)

density

1.072 g/mL at 25 °C (lit.)

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)

Articles

The synthesis of biaryl compounds via the Suzuki–Miyaura coupling reaction has become more commonplace now that many arylboronic acids are readily available.

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