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885051-07-0,MFCD11112169
Catalog No.:AA003B9K

885051-07-0 | (+)-Benzotetramisole

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Purity
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100mg
98% 99%ee
in stock  
$22.00   $15.00
- +
250mg
98% 99%ee
in stock  
$26.00   $18.00
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1g
98% 99%ee
in stock  
$84.00   $59.00
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5g
98% 99%ee
in stock  
$417.00   $292.00
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  • Technical Information
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  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA003B9K
Chemical Name:
(+)-Benzotetramisole
CAS Number:
885051-07-0
Molecular Formula:
C15H12N2S
Molecular Weight:
252.3342
MDL Number:
MFCD11112169
SMILES:
c1ccc(cc1)[C@H]1N=c2n(C1)c1c(s2)cccc1
Properties
Properties
 
Form:
Solid  
MP:
95.0-95.5℃ (ethyl ether hexane )  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
348  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
18  
Hydrogen Bond Acceptor Count:
2  
Rotatable Bond Count:
1  
XLogP3:
3.2  

Literature

Title: Origin of enantioselectivity in benzotetramisole-catalyzed dynamic kinetic resolution of azlactones.

Journal: Organic letters 20120706

Title: Kinetic resolution of α-substituted alkanoic acids promoted by homobenzotetramisole.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20110926

Title: Kinetic resolution of N-acyl-β-lactams via benzotetramisole-catalyzed enantioselective alcoholysis.

Journal: Journal of the American Chemical Society 20110907

Title: Kinetic resolution of racemic alpha-arylalkanoic acids with achiral alcohols via the asymmetric esterification using carboxylic anhydrides and acyl-transfer catalysts.

Journal: Journal of the American Chemical Society 20100825

Title: Benzotetramisole-catalyzed dynamic kinetic resolution of azlactones.

Journal: Organic letters 20100219

Title: Homobenzotetramisole: an effective catalyst for kinetic resolution of aryl-cycloalkanols.

Journal: Organic letters 20080320

Title: Kinetic resolution of propargylic alcohols catalyzed by benzotetramisole.

Journal: Organic letters 20061012

Title: Benzotetramisole: a remarkably enantioselective acyl transfer catalyst.

Journal: Organic letters 20060330

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SDS
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