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(R)-(+)-N,N-Dimethyl-1-ferrocenylethylamine
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(R)-(+)-N,N-Dimethyl-1-ferrocenylethylamine

CAS: 31886-58-5

Ref. 3D-GBA88658

1gDiscontinued
5gDiscontinued
10gDiscontinued
250mgDiscontinued
500mgDiscontinued

Discontinued product. For inquiries about similar products, please fill out our form or email us at .


Product Information

Name:
(R)-(+)-N,N-Dimethyl-1-ferrocenylethylamine
Synonyms:
  • (R)-(-)-N,N-Dimethyl-1-ferrocenyl ethylamine
  • (R)-(1-N,N-Dimethylaminoethyl)ferrocene
  • (R)-1-(Dimethylamino)-1-ferrocenylethane
  • (R)-[1-(Dimethylamino)ethyl]ferrocene
  • 1-cyclopenta-2,4-dienyl-[2-[(1R)-1-dimethylaminoethyl]-1-cyclopenta-2,4-dienyl]iron
  • Ferrocene, [(1R)-1-(dimethylamino)ethyl]-
  • Ferrocene, [1-(dimethylamino)ethyl]-, (R)-
  • Ferrocenemethylamine, N,N,α-trimethyl-, (R)-(+)-
  • Ugi's amine
  • [(1R)-1-(Dimethylamino)ethyl]ferrocene
  • See more synonyms
Description:

(R)-(+)-N,N-Dimethyl-1-ferrocenylethylamine is a chiral catalyst that is used in the transfer hydrogenation of olefins. It also has asymmetric properties. This agent catalyzes the transfer of one hydrogen atom to an olefinic double bond and can be used for reductive amination reactions. (R)-(+)-N,N-Dimethyl-1-ferrocenylethylamine can be used for the synthesis of esters from acetyl chloride and alcohols, as well as for Friedel-Crafts reactions with aromatic compounds. The mechanism of this process is not fully understood but it is thought that nucleophilic attack by this agent on the carbonyl group leads to formation of an intermediate carbocation that reacts with a second molecule of the alcohol or phenol to form an ester or ketone respectively.

Notice:
Our products are intended for lab use only. For any other use, please contact us.
Brand:
Biosynth
Long term storage:
Notes:

Chemical properties

Molecular weight:
257.16 g/mol
Formula:
C14H19FeN
Purity:
Min. 95%
MDL:
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Concentration:
EINECS:
Merck:
HS code:

Hazard Info

UN Number:
EQ:
Class:
H Statements:
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Forbidden to fly:
Hazard Info:
Packing Group:
LQ:

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