261165-25-7

Basic information

• Product Name: [(1R)-2-methyl-1-[[(3aR,6S,7aS)-tetrahydro-8,8-dimethyl-2,2-dioxide-3H-3a,6-methano-2,1-benzisothiazol-1(4H)-yl]carbonyl]propyl]carbamic acid 2,2-dioxide phenylmethyl ester
• Synonyms: [(1R)-2-methyl-1-[[(3aR,6S,7aS)-tetrahydro-8,8-dimethyl-2,2-dioxide-3H-3a,6-methano-2,1-benzisothiazol-1(4H)-yl]carbonyl]propyl]carbamic acid 2,2-dioxide phenylmethyl ester
• CAS NO: 261165-25-7
• Molecular Weight: 448.583
• Mol File: 261165-25-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: [(1R)-2-methyl-1-[[(3aR,6S,7aS)-tetrahydro-8,8-dimethyl-2,2-dioxide-3H-3a,6-methano-2,1-benzisothiazol-1(4H)-yl]carbonyl]propyl]carbamic acid 2,2-dioxide phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: [(1R)-2-methyl-1-[[(3aR,6S,7aS)-tetrahydro-8,8-dimethyl-2,2-dioxide-3H-3a,6-methano-2,1-benzisothiazol-1(4H)-yl]carbonyl]propyl]carbamic acid 2,2-dioxide phenylmethyl ester(261165-25-7)
• EPA Substance Registry System: [(1R)-2-methyl-1-[[(3aR,6S,7aS)-tetrahydro-8,8-dimethyl-2,2-dioxide-3H-3a,6-methano-2,1-benzisothiazol-1(4H)-yl]carbonyl]propyl]carbamic acid 2,2-dioxide phenylmethyl ester(261165-25-7)

Safety Data

• Hazardous Substances Data: 261165-25-7(Hazardous Substances Data)

Upstream product

• 623924-86-7 (3aR,6S,7aS)-hexahydro-8,8-dimethyl-1-[(2R)-1-oxo-2-(2,2-diphenylhydrazino)-3-(methyl)butyl]-3H-3a,6-methano-2,1-benzisothiazole 2,2-dioxide 
• 261165-24-6 (R)-2-Benzyloxyamino-1-((1R,5S,7S)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-3-methyl-butan-1-one 
• 623924-85-6 1-((1R,5S,7S)-10,10-Dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-2-(diphenyl-hydrazono)-ethanone 
• 108448-77-7 (+)-camphorsultam 
• 501-53-1 benzyl chloroformate 
• 261168-61-0 (R)-2-Amino-1-((1R,5S,7S)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-3-methyl-butan-1-one 

Downstream Products

• 1685-33-2 N-[(benzyloxy)carbonyl]-D-valine 

Relevant articles and documents

Asymmetric synthesis ofa-amino acids: Indium-mediated reactions of glyoxylic oxime ether in aqueous media

The indium-mediated allylation and alkylation reactions of the Oppolzer camphorsultam derivative of glyoxylic oxime ether proceeded with excellent diastereoselectivity in aqueous media, providing a variety of enantiomerically purea-amino acids.

Zinc-mediated radical reaction of glyoxylic oxime ether and hydrazone in aqueous media: Asymmetric synthesis of α-amino acids

Alkyl radical addition to glyoxylic oxime ether and hydrazone in aqueous media was studied using zinc dust as a radical initiator. The zinc-mediated radical reaction of the hydrazone bearing a chiral camphorsultam provided the corresponding alkylated prod