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807885

Sigma-Aldrich

Ac-Tle-OH

Synonym(s):

(2S)-2-Acetamido-3,3-dimethylbutanoic acid, N-α-Acetyl-L-tert-leucine, N-Acyl-tert-Leucine

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About This Item

Empirical Formula (Hill Notation):
C8H15NO3
CAS Number:
22146-59-4
Molecular Weight:
173.21
MDL number:
MFCD08275827
UNSPSC Code:
12352300
PubChem Substance ID:
329768752
NACRES:
NA.22

Assay

95%

Quality Level

100

form

powder

mp

230 °C

SMILES string

O=C(O)[C@H](C(C)(C)C)NC(C)=O

InChI

1S/C8H15NO3/c1-5(10)9-6(7(11)12)8(2,3)4/h6H,1-4H3,(H,9,10)(H,11,12)/t6-/m1/s1

InChI key

WPPXAQGLXQAVTE-ZCFIWIBFSA-N

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
MKBW6806V

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Yu Group – Professor Product Portal

The Yu program centers around the discovery of catalytic carbon–carbon and carbon–heteroatom bond forming reactions based on C–H activation. Target transformations are selected to enable 1) the use of simple and abundant starting materials such as aliphatic acids, amines and alcohols, and 2) disconnections that drastically shorten the synthesis of a drug molecule or a major class of biologically active compounds.

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