127556-03-0

Basic information

• Product Name: (2R)-BORNANE-10,2-SULTAM GLYCINATE
• Synonyms: (2R)-BORNANE-10,2-SULTAM GLYCINATE
• CAS NO: 127556-03-0
• Molecular Formula: C₁₅H₂₄N₂O₃S₃
• Molecular Weight: 376.56
• Mol File: 127556-03-0.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (2R)-BORNANE-10,2-SULTAM GLYCINATE(CAS DataBase Reference)
• NIST Chemistry Reference: (2R)-BORNANE-10,2-SULTAM GLYCINATE(127556-03-0)
• EPA Substance Registry System: (2R)-BORNANE-10,2-SULTAM GLYCINATE(127556-03-0)

Safety Data

• Hazardous Substances Data: 127556-03-0(Hazardous Substances Data)

Usage

General Description

(2R)-Bornane-10,2-sultam glycinate is a chemical compound with a molecular formula of C10H18N2O7S and a molecular weight of 302.32 g/mol. It is a white crystalline powder that is soluble in water and has a melting point of 206-208°C. (2R)-BORNANE-10,2-SULTAM GLYCINATE is used in the pharmaceutical industry as an intermediate in the synthesis of various medications. It is also used in the production of fine chemicals and polymers. The (2R)-configuration of the compound indicates that it has a specific arrangement of atoms in its structure, which can affect its properties and reactivity. Overall, (2R)-bornane-10,2-sultam glycinate is a versatile compound with various applications in the chemical and pharmaceutical industries.

Upstream product

• 332041-85-7 [3aR-[(3aS*,4S*,6aR*),3aα,6α,7aβ]]-3H-3a,6-methano-2,1-benzisothiazole, hexahydro-8,8-dimethyl-4-[[tetrahydro-1,3-dioxolo-5-(phenylmethyl)-2-oxo-[4,5-c]-pyrrol-4-yl]carbonyl]-2,2-dioxide 
• 332041-84-6 [3aR-[(3aR*,4R*,6aS*),3aα,6α,7aβ]]-3H-3a,6-methano-2,1-benzisothiazole, hexahydro-8,8-dimethyl-4-[[tetrahydro-1,3-dioxolo-5-(phenylmethyl)-2-oxo-[4,5-c]-pyrrol-4-yl]carbonyl]-2,2-dioxide 
• 332041-80-2 [3aR-[1(2R*,3R*),3aα,6α,7aβ]]-3-pyrrolidine-carboxylic acid, 1-(phenylmethyl)-2-[(tetrahydro-8,8-dimethyl-3H-3a,6-methano-2,1-benzisothiazol-1(4H)-yl)-carbonyl]-methyl ester, S,S-dioxide 
• 635678-42-1 (1R,2S,4S)-N-(2,3-dibromopropionyl)-bornane-2,10-sultam 
• 153440-80-3 ((R)-1-Benzyl-aziridin-2-yl)-((1R,5S,7S)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-methanone 
• 119944-89-7 (2S)-N-(acryloyl)bornane-10,2-sultam 
• 58091-08-0 methyl N-(bis(methyl)thiomethilene)glycinate 
• 108448-77-7 (+)-camphorsultam 

Downstream Products

• 443126-84-9 C₂₄H₃₂N₂O₃S₃ 
• 137718-68-4 Carbonic acid (Z)-4-[[(R)-1-((1R,5S,7S)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]decane-4-carbonyl)-but-3-enyl]-(2,4,6-trimethyl-benzenesulfonyl)-amino]-but-2-enyl ester methyl ester 
• 137718-74-2 (3R,4aR,7aR)-3-((1R,5S,7S)-10,10-Dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]decane-4-carbonyl)-7-methyl-2-(2,4,6-trimethyl-benzenesulfonyl)-octahydro-[2]pyrindin-6-one 
• 137718-69-5 (3R,4aR,7aR)-3-((1R,5S,7S)-10,10-Dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]decane-4-carbonyl)-7-methylene-2-(2,4,6-trimethyl-benzenesulfonyl)-octahydro-[2]pyrindin-6-one 
• 137718-67-3 N-[(R)-1-((1R,5S,7S)-10,10-Dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]decane-4-carbonyl)-but-3-enyl]-2,4,6-trimethyl-benzenesulfonamide 
• 94594-90-8 (2R)-bornane-10,2-sultam 
• 161264-10-4 (2R)-N-<(2S)-6--2-<amino>hexanoyl>bornane-10,2-sultam 
• 161264-09-1 (2R)-N-<(2S)-5--2-<amino>pentanoyl>bornane-10,2-sultam 
• 161264-12-6 (2R)-N-<(2S)-2-<amino>-6-(N-phenyl-N-tosylamino)-hexanoyl>bornane-10,2-sultam 
• 161264-14-8 (2R)-N-<(2S)-8-<(benzyloxycarbonyl)amino>-2-<amino>octanoyl>bornane-10,2-sultam 
• 161264-11-5 (2R)-N-<(2S)-6--2-<amino>hexanoyl>bornane-10,2-sultam 
• 161264-13-7 (2R)-N-<(2S)-7-<(benzyloxycarbonyl)amino>2-<amino>heptanoyl>bornane-10,2-sultam 
• 127556-12-1 N-<(S)-2'-amino-3-phenylpropanoyl>bornane-2,10-sultam hydrochloride 
• 108448-77-7 (+)-camphorsultam 

Relevant articles and documents

Stereocontrolled 1,3-dipolar cycloadditions using Oppolzer's camphor sultam as the chiral auxiliary for carbonyl stabilized azomethine ylides

Two complementary approaches to substituted pyrrolidines via stereocontrolled 1,3-dipolar cycloaddition reactions of chiral azomethine ylides are described. In one approach, chiral azomethine ylides were generated by thermolysis of aziridine carboxylate sultams and trapped with a variety of dipolarophiles to give good yields of the corresponding cycloadducts. In the second approach, chiral azomethine ylides were generated from glycyl sultams by 'imine tautomerization' and trapped with dipolarophiles to give good yields of the corresponding cycloadducts.