Skip to Content
Merck
All Photos(1)

Key Documents

687340

Sigma-Aldrich

N-Boc-4,4-difluoro-L-proline

97%

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C10H15F2NO4
CAS Number:
Molecular Weight:
251.23
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

form

solid

optical activity

[α]22/D -69.0° in chloroform

mp

120-124 °C

functional group

carboxylic acid
fluoro

SMILES string

CC(C)(C)OC(=O)N1CC(F)(F)C[C@H]1C(O)=O

InChI

1S/C10H15F2NO4/c1-9(2,3)17-8(16)13-5-10(11,12)4-6(13)7(14)15/h6H,4-5H2,1-3H3,(H,14,15)/t6-/m0/s1

InChI key

WTMZYKCXBXPVPT-LURJTMIESA-N

Application

N-Boc-4,4-difluoro-L-proline can be used as a substrate in the preparation of possible dipeptidyl peptidase I (DPPI) inhibitors and VLA-4 antagonists.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

4-(Pyrrolidinyl) methoxybenzoic acid derivatives as a potent, orally active VLA-4 antagonist
Chiba J, et al.
Chemical & Pharmaceutical Bulletin, 54(11), 1515-1529 (2006)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service