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About This Item
Empirical Formula (Hill Notation):
C7H12N2O2
CAS Number:
Molecular Weight:
156.18
Beilstein:
82869
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
97%
optical activity
[α]20/D −31.5°, c = 1 in H2O
mp
258-262 °C (lit.)
SMILES string
CC(C)[C@H]1NC(=O)CNC1=O
InChI
1S/C7H12N2O2/c1-4(2)6-7(11)8-3-5(10)9-6/h4,6H,3H2,1-2H3,(H,8,11)(H,9,10)/t6-/m1/s1
InChI key
IULFBTHVPRNQCG-ZCFIWIBFSA-N
Application
Chiral auxiliary developed by Professor Schöllkopf for the enantioselective synthesis of α-amino acids.
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
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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Find documentation for the products that you have recently purchased in the Document Library.
Rose, J.E. et al.
Journal of the Chemical Society. Perkin Transactions 1, 157-157 (1995)
Schollkopf, U. et al.
Angewandte Chemie (International Edition in English), 20, 798-798 (1981)
Rose, J.E. et al.
Journal of the Chemical Society. Perkin Transactions 1, 1563-1563 (1992)
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