(1S)-(-)-2,10-Camphorsultam, 98%

Code: 298352-5G D2-231

Application

(1S)-(−)-2,10-Camphorsultam may be used in the asymmetric synthesis of (S)- and (R)-N-Fmoc-S-trityl-α-methylcysteine....


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€159.00 5G
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Application

(1S)-(−)-2,10-Camphorsultam may be used in the asymmetric synthesis of (S)- and (R)-N-Fmoc-S-trityl-α-methylcysteine. It may be used as proton source in the synthesis of chiral α,γ-substituted γ-butyrolactones.

General description

(1S,2R,4R)-(−)-2,10-Camphorsultam may be employed as a chiral probe for the optical resolution by HPLC and X-ray crystallographic determination of the absolute stereochemistry of carboxylic acids.

Packaging

5 g in glass bottle

assay98%
formsolid
InChI keyDPJYJNYYDJOJNO-NQMVMOMDSA-N
InChI1S/C10H17NO2S/c1-9(2)7-3-4-10(9)6-14(12,13)11-8(10)5-7/h7-8,11H,3-6H2,1-2H3/t7-,8-,10-/m1/s1
mp181-183 °C (lit.)
optical activity[α]19/D −32°, c = 5 in chloroform
Quality Level200
SMILES string[H][C@@]12CC[C@]3(CS(=O)(=O)N[C@@H]3C1)C2(C)C
Cas Number94594-90-8
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