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Safety Information

434639

Sigma-Aldrich

(S)-(+)-2,2-Dimethylcyclopropanecarboxamide

98%

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About This Item

Linear Formula:
(CH3)2C3H3CONH2
CAS Number:
Molecular Weight:
113.16
EC Number:
MDL number:
UNSPSC Code:
12352111
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

form

solid

optical activity

[α]20/D +82°, c = 1 in methanol

mp

135-137 °C (lit.)

SMILES string

CC1(C)C[C@@H]1C(N)=O

InChI

1S/C6H11NO/c1-6(2)3-4(6)5(7)8/h4H,3H2,1-2H3,(H2,7,8)/t4-/m1/s1

InChI key

YBZQRYWKYBZZNT-SCSAIBSYSA-N

Application

Employed in the preparation of (Z)-2-(acylamino)-3-substituted propenoic acids as inhibitors of the mammalian β-lactamase renal dipeptidase.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - 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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

434639-BULK:
434639-1KG:
434639-VAR:
434639-10G:
434639-100G:
434639-1G:


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D W Graham et al.
Journal of medicinal chemistry, 30(6), 1074-1090 (1987-06-01)
The title enzyme deactivates the potent carbapenem antibiotic imipenem in the kidney, producing low antibiotic levels in the urinary tract. A series of (Z)-2-(acylamino)-3-substituted-propenoic acids (3) are specific, competitive inhibitors of the enzyme capable of increasing the urinary concentration of

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