ChemAbout
© 2026 ChemAbout
Insights|Política de Privacidade|Termos de Uso|[email protected]
Início/Compostos/Reagente de pesquisa/(S)-RUCY(regR)-XylBINAP
C71H73ClN2O2P2Ru
1184.8 g/mol
Reagente de pesquisaPerigo

(S)-RUCY(regR)-XylBINAP

CAS1312713-89-5EC811-492-9
Categoria
Reagente de pesquisa
Classe do Composto
Organometálico
Uso Principal
Composto de pesquisa

(S)-RUCY(regR)-XylBINAP is a ruthenium-based organometallic compound employed as a catalyst in asymmetric hydrogenation reactions. It is primarily used for research purposes, particularly in the development of enantioselective synthetic methods.

asymmetric hydrogenation catalystresearch reagent for enantioselective synthesis

Escopo do conteúdo: As informações desta página dizem respeito à identificação química e aos contextos de fornecimento industrial, pesquisa e produção. Não constituem alegação terapêutica, aconselhamento médico ou instruções de uso de medicamentos.

Adquirindo ou fornecendo este composto?

Publique seu inventário ou uma solicitação de compra

CAS 1312713-89-5

Publicar este produto
Faça login para publicar informações de fornecimento
Solicitar este produto
Envie uma solicitação sem se registrar

Compostos relacionados

ForteMesma estrutura base

(R)-(+)-2,2'-BIS[DI(3,5-XYLYL)PHOSPHINO]-1,1'-BINAPHTHYL

CAS135139-00-3

chiral ligand for asymmetric catalysis

ForteMesma estrutura base

(R)-(+)-2,2'-BIS[DI(3,5-XYLYL)PHOSPHINO]-1,1'-BINAPHTHYL

CAS137219-86-4

chiral phosphine ligand for catalysis

ForteMesma estrutura base

RUCL2[(S)-XYLBINAP][(S,S)-DPEN]

CAS220114-03-4

asymmetric hydrogenation catalyst

ForteMesma estrutura base

RuCl2[(R)-xylbinap][(R)-daipen]

CAS220114-32-9

asymmetric hydrogenation catalyst

ReferênciaMesma categoria

Tri-tert-butylphosphine tetrafluoroborate

CAS131274-22-1

ligand precursor for cross-coupling reactions

ReferênciaMesma categoria

Neopentylmagnesium chloride

CAS13132-23-5

Grignard reagent for organic synthesis

ReferênciaMesma categoria

(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-6-amino-2-[[(2S)-5-amino-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-6-amino-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-amino-3-carboxypropanoyl]amino]-3-hydroxypropanoyl]amino]-4-methylpentanoyl]amino]hexanoyl]amino]-3-hydroxypropanoyl]amino]-3-(4-hydroxyphenyl)propanoyl]amino]-3-(1H-indol-3-yl)propanoyl]amino]-3-(4-hydroxyphenyl)propanoyl]amino]-4-methylpentanoyl]amino]-5-oxopentanoyl]amino]hexanoyl]amino]-3-phenylpropanoyl]amino]-3-hydroxypropanoyl]amino]-3-(1H-indol-3-yl)propanoyl]amino]-5-carbamimidamidopentanoic acid

CAS1313390-49-6

research peptide

ReferênciaMesma categoria

2-(3-bromophenyl)triphenylene

CAS1313514-53-2

research compound

Referência de Segurança

Nocivo
Nocivo
Risco à saúde
Risco à saúde
Perigo
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
H340May cause genetic defects
H360May damage fertility or the unborn child
H371May cause damage to organs
H373May cause damage to organs through prolonged or repeated exposure
Identificadores
Nome IUPAC

[1-[2-bis(3,5-dimethylphenyl)phosphanylnaphthalen-1-yl]naphthalen-2-yl]-bis(3,5-dimethylphenyl)phosphane;chlororuthenium(1+);(2S)-1-(4-methoxybenzene-6-id-1-yl)-1-(4-methoxyphenyl)-3-methylbutane-1,2-diamine

InChIKey

IQWRCNFONDXTCS-UCPQXOCLSA-M

SMILES

CC1=CC(=CC(=C1)P(C2=C(C3=CC=CC=C3C=C2)C4=C(C=CC5=CC=CC=C54)P(C6=CC(=CC(=C6)C)C)C7=CC(=CC(=C7)C)C)C8=CC(=CC(=C8)C)C)C.CC(C)[C@@H](C(C1=CC=C(C=C1)OC)(C2=[C-]C=C(C=C2)OC)N)N.Cl[Ru+]

Sinônimos (2)
  • (S)-RUCY(TM)-XylBINAP
  • (S)-RUCY(regR)-XylBINAP