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About This Item
Empirical Formula (Hill Notation):
C7H12N2O2
CAS Number:
Molecular Weight:
156.18
Beilstein/REAXYS Number:
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
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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