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(2S)-Bornane-10,2-sultam

(2S)-Bornane-10,2-sultam Structure
(2S)-Bornane-10,2-sultam structure
CAS No.
108448-77-7
Chemical Name:
(2S)-Bornane-10,2-sultam
Synonyms
(7aS)-8,8-Dimethylhexahydro-1H-3a,6-methanobenzo[c]isothiazole 2,2-dioxide;2-sultaM;L-SultaM;(2S)-Bornane-10;L-2,10-amphorsultam;D-(-)-CAMPHOR SULTAM;(+)-10,2-CAMPHORSULTAM;(+)-2,10-CAMPHORSULTAM;(1R)-(+)-Camphorsultam;(2S)-Borne-10,2-sultam
CBNumber:
CB2411257
Molecular Formula:
C10H17NO2S
Molecular Weight:
215.31
MDL Number:
MFCD00151762
MOL File:
108448-77-7.mol
MSDS File:
SDS
Last updated:2023-04-27 16:27:43
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(2S)-Bornane-10,2-sultam Properties

Melting point 185-187 °C(lit.)
alpha 33 º (c=4.9, CHCl3)
Boiling point 324.8±25.0 °C(Predicted)
Density 1.1469 (rough estimate)
refractive index 31 ° (C=1, CHCl3)
storage temp. Sealed in dry,Room Temperature
solubility almost transparency in Chloroform
form powder to crystal
pka 11.05±0.40(Predicted)
color White to Almost white
optical activity [α]20/D +32°, c = 5 in chloroform
BRN 4675755
InChIKey DPJYJNYYDJOJNO-CFGJQEBVSA-N
CAS DataBase Reference 108448-77-7(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P280a-P304+P340-P405-P501a-P261-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36-37/39
WGK Germany  3
HS Code  29242990
NFPA 704
1
2 0

(2S)-Bornane-10,2-sultam price More Price(46)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical C1324 (+)-10,2-Camphorsultam >98.0%(GC) 108448-77-7 1g $94 2021-12-16 Buy
TCI Chemical C1324 (+)-10,2-Camphorsultam >98.0%(GC) 108448-77-7 5g $325 2024-03-01 Buy
Alfa Aesar A14133 (1R,2S)-(+)-10,2-Camphorsultam, 99% 108448-77-7 1g $75.65 2024-03-01 Buy
Alfa Aesar A14133 (1R,2S)-(+)-10,2-Camphorsultam, 99% 108448-77-7 5g $237.65 2024-03-01 Buy
TRC C175130 (1R)-(+)-2,10-Camphorsultam 108448-77-7 10g $215 2021-12-16 Buy
Product number Packaging Price Buy
C1324 1g $94 Buy
C1324 5g $325 Buy
A14133 1g $75.65 Buy
A14133 5g $237.65 Buy
C175130 10g $215 Buy

(2S)-Bornane-10,2-sultam Chemical Properties,Uses,Production

Chemical Properties

white to light yellow crystal powde

Uses

(1R)-(+)-2,10-Camphorsultam has been used as a reactant in the synthesis of pyrrolidine acid analogs as potent dual PPARα/γ agonists.

Purification Methods

The (-)-enantiomer is recrystallised from 95% EtOH and dried in a vacuum desiccator. It dissolves in dilute aqueous NaOH and can be precipitated without hydrolysis by acidifying. It forms the N-Na salt in EtOH (by addition of Na to the EtOH solution), and the salt can be methylated with MeI to give the (-)-N-Me lactam with m 80o after recrystallisation from hot H2O and has []D -59.6o (c 5, CHCl3) [Shriner et al. J Am Chem Soc 60 2794 1938]. [Oppolzer et al. Helv Chim Acta 69 1142 1986, Weismiller et al. Org Synth 69 154 1955, Beilstein 27 III/IV 1007.]

(2S)-Bornane-10,2-sultam synthesis

107869-45-4
108448-77-7
Synthesis of (2S)-Bornane-10,2-sultam from (+)-10-CAMPHORSULFONIMINE

(2S)-Bornane-10,2-sultam Preparation Products And Raw materials

Raw materials

Preparation Products

(+)-10-CAMPHORSULFONIMINE

(2S)-Bornane-10,2-sultam Suppliers

Global( 268)Suppliers
Supplier Tel Email Country ProdList Advantage
Changzhou Chontech Baocheng Chemical Co.,Ltd
+86-51982698291; +undefined15295095616 info@hhbhswkj.com China 73 58
Capot Chemical Co.,Ltd. 		571-85586718 +8613336195806 sales@capotchem.com China 29797 60
Shanghai Daken Advanced Materials Co.,Ltd 		+86-371-66670886 info@dakenam.com China 15933 58
ATK CHEMICAL COMPANY LIMITED 		+undefined-21-51877795 ivan@atkchemical.com China 32480 60
career henan chemical co 		+86-0371-86658258 sales@coreychem.com China 29914 58
Hubei Jusheng Technology Co.,Ltd. 		18871490254 linda@hubeijusheng.com CHINA 28180 58
Accela ChemBio Inc. 		(+1)-858-699-3322 info@accelachem.com United States 19965 58
Xi'an Kono chem co., Ltd., 		029-86107037 13289246953 info@konochemical.com China 2995 58
Hubei xin bonus chemical co. LTD 		86-13657291602 linda@hubeijusheng.com CHINA 22968 58
Chongqing Chemdad Co., Ltd 		+86-023-61398051 +8613650506873 sales@chemdad.com China 39916 58
Supplier Advantage
Changzhou Chontech Baocheng Chemical Co.,Ltd
58
Capot Chemical Co.,Ltd. 		60
Shanghai Daken Advanced Materials Co.,Ltd 		58
ATK CHEMICAL COMPANY LIMITED 		60
career henan chemical co 		58
Hubei Jusheng Technology Co.,Ltd. 		58
Accela ChemBio Inc. 		58
Xi'an Kono chem co., Ltd., 		58
Hubei xin bonus chemical co. LTD 		58
Chongqing Chemdad Co., Ltd 		58

View Lastest Price from (2S)-Bornane-10,2-sultam manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
(1R)-(+)-2,10-Camphorsultam pictures 2023-02-18 (1R)-(+)-2,10-Camphorsultam
108448-77-7
 US $0.00-0.00 / kg 1kg 98% kgs Aromsyn Co., Ltd.
(2S)-Bornane-10,2-sultam pictures 2022-08-25 (2S)-Bornane-10,2-sultam
108448-77-7
 US $1.10 / g 1g 99.00% 100 Tons Min Dideu Industries Group Limited
(2S)-Bornane-10,2-sultam pictures 2019-07-06 (2S)-Bornane-10,2-sultam
108448-77-7
 US $1.00 / KG 1KG 98% 20KG Career Henan Chemical Co

(2S)-Bornane-10,2-sultam Spectrum

(2S)-Bornane-10,2-sultam(108448-77-7)MS(2S)-Bornane-10,2-sultam(108448-77-7)1HNMR(2S)-Bornane-10,2-sultam(108448-77-7)13CNMR(2S)-Bornane-10,2-sultam(108448-77-7)IR1(2S)-Bornane-10,2-sultam(108448-77-7)IR2(2S)-Bornane-10,2-sultam(108448-77-7)Raman

108448-77-7((2S)-Bornane-10,2-sultam)Related Search:

3-Aminobenzenesulfonamide N,N-Dimethylformamide Dacthal Dimethyl ether Dimethyl sulfoxide
Methanesulfonamide Cyclopropanesulfonamide Dimethyl fumarate Sulfanilamide Benzenesulfonamide
Dimethyl carbonate ETHANE Dimethyl sulfate Dimethyl phthalate Dimethyl disulfide
p-Toluenesulfonamide (2R)-Bornane-10,2-sultam (1S)-(+)-10-CAMPHORSULFONAMIDE

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L-2,10-Camphorsultam,99%e.e. (2S)-BORNANE-10,2-SULTAM (1R)-(+)-2,10-CAMPHORSULTAM (1R)-2,10-CAMPHORSULTAM (1R,2S)-(+)-2,10-CAMPHORSULTAM (1R,5S)-10,10-DIMETHYL-3-THIA-4-AZATRICYCLO[5.2.1.01,5]DECANE 3,3-DIOXIDE (+)-2,10-CAMPHORSULTAM (+)-10,2-CAMPHORSULTAM (IR)-(+)-2,10-Camphorsultam (1R)-(+)-2,10-camphorsultam ,98% L-2,10-amphorsultam (2S)-Bornane-10 2-sultaM (2S)-Bornane-1,2-sultaM L-SultaM (2S)-Bornane-10,2-sultam (1R,5S)-10,10-Dimethyl-3-thia-4-azatricyclo[5.2.1.0(1,5)]decane 3,3-Dioxide (1R)-(+)-2,10-Camphorsultam (5S,7S)-10,10-dimethyl-3λ-thia-4-azatricyclo[5.2.1.01,]decane-3,3-dione (2S)-Bornane-10,2-sultam (1R)-(+)-2,10-Camphorsultam [3AR-(3A-ALPHA,6-ALPHA,7A-BETA)]-HEXAHYDRO-8,8-DIMETHYL-2,2-DIOXIDE-3H-3A,6-METHANO-2,1-BENZISOTHIAZOLE [3aR-(3aalpha,6alpha,7abeta)]-Hexahydro-8,8-dimethyl-2,2-dioxide-3H-3a,6-methano-2,1-benzisothiazole (+)-EXO-10,2-BORNANESULTAM (+)-L-2,10-CAMPHORSULTAM L(+)-10,2-CAMPHORSULTAME D-(-)-CAMPHOR SULTAM (+)-2,10-CAMPHORSULTAM 99% (2S)-Bornane-10,2-sultam,99+%, (99+% ee) (2S)-Bornane-10,2-sultam,98% (+)-exo-10,2-Bornanesultam, (1R,5S)-10,10-Dimethyl-3-thia-4-azatricyclo[5.2.1.01,5]decane 3,3-dioxide (+)-10,2-Camphorsultam, (+)-exo-10,2-Bornanesultam, L-2,10-Camphorsultam, (1R,5S)-10,10-Dimethyl-3-thia-4-azatricyclo[5.2.1.01,5]decane 3,3-dioxide (1β,5α,7β)-10,10-Dimethyl-3-thia-4-azatricyclo[5.2.1.01,5]decane3,3-dioxide (3aR)-1,4,5,6,7,7aβ-Hexahydro-8,8-dimethyl-3H-3aα,6α-methano-2,1-benzisothiazole 2,2-dioxide (3aR,3aα,6α,7aβ)-8,8-Dimethyl-3a,6-methanooctahydro-2,1-benzisothiazole 2,2-dioxide [3aR,7aβ,(+)]-Hexahydro-8,8-dimethyl-3H-3aα,6α-methano-2,1-benzisothiazole 2,2-dioxide (1R)-(+)-Camphorsultam (1R,2S)-(+)-10,2-Camphorsultam (2S)-Borne-10,2-sultam (1R,2S)-(+)-10,2-CamphorsuL 3H-3a,6-Methano-2,1-benzisothiazole, hexahydro-8,8-dimethyl-, 2,2-dioxide, (3aR,6S,7aS)- (3aR)-8,8-dimethylhexahydro-2H-3a,6-methanobenzo[d]isothiazole 1,1-dioxide (2S)-Bornane-10,2-sultam ISO 9001：2015 REACH (3aR,6S,7aS)-8,8-Dimethylhexahydro-1H-3a,6-methanobenzo[c]isothiazole 2,2-dioxide (7aS)-8,8-Dimethylhexahydro-1H-3a,6-methanobenzo[c]isothiazole 2,2-dioxide (+)-10，2-Camphorsultam (5S,7S)-10,10-dimethyl-3λ?-thia-4-azatricyclo[5.2.1.01?]decane 3,3-dioxide (+)-2,10-Camphorsultam 108448-77-7 C10H17NO2S Sulfur-Based Sulfur Compounds (for Synthesis) Bicyclic Monoterpenes Terpenes Asymmetric Synthesis Chiral Auxiliaries chiral Asymmetric Synthesis Bicyclic Monoterpenes Biochemistry