21612
L-(−)-α-Amino-ε-caprolactam hydrochloride
≥97.0% (AT)
Synonym(s):
(S)-3-Amino-hexahydro-2-azepinone hydrochloride, L-Lysine lactam hydrochloride
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About This Item
Empirical Formula (Hill Notation):
C6H12N2O · HCl
CAS Number:
Molecular Weight:
164.63
UNSPSC Code:
12352005
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
4820243
Product Name
L-(−)-α-Amino-ε-caprolactam hydrochloride, ≥97.0% (AT)
InChI
1S/C6H12N2O.ClH/c7-5-3-1-2-4-8-6(5)9;/h5H,1-4,7H2,(H,8,9);1H/t5-;/m0./s1
SMILES string
Cl[H].N[C@H]1CCCCNC1=O
InChI key
LWXJCGXAYXXXRU-JEDNCBNOSA-N
assay
≥97.0% (AT)
form
solid
optical activity
[α]20/D −27±2°, c = 1% in H2O
optical purity
enantiomeric ratio: ≥99:1 (HPLC)
storage temp.
2-8°C
Quality Level
Related Categories
Application
L-(−)-α-Amino-ε-caprolactam hydrochloride can be used to introduce caprolactam moiety during the total synthesis of bengamides, which are bioactive compounds naturally found in marine sponges.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Total synthesis of bengamide E and analogues by modification at C-2 and at terminal olefinic positions
Sarabia F and S'anchez-Ruiz A
The Journal of Organic Chemistry, 70(23), 9514-9520 (2005)
Total synthesis of bengamide E
Liu W, et al.
Tetrahedron Letters, 43(8), 1373-1375 (2002)
A diversity-oriented synthetic approach to bengamides
Sarabia F and S'anchez-Ruiz A
Tetrahedron Letters, 46(7), 1131-1135 (2005)
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