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Key Documents

L511269

Sigma-Aldrich

2,2′-Azanediyldibenzonitrile

AldrichCPR

동의어(들):

2-2′-Iminobis-benzonitrile, Yu-Li Auxiliary

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About This Item

실험식(Hill 표기법):
C14H9N3
CAS Number:
Molecular Weight:
219.24
MDL number:
UNSPSC 코드:
12161600
PubChem Substance ID:

Quality Level

반응 적합성

reagent type: catalyst
reagent type: ligand
reaction type: C-H Activation

SMILES string

N#Cc1ccccc1Nc2ccccc2C#N

InChI

1S/C14H9N3/c15-9-11-5-1-3-7-13(11)17-14-8-4-2-6-12(14)10-16/h1-8,17H

InChI key

JGNDVMNUMRWBSN-UHFFFAOYSA-N

애플리케이션

Application of tethered nitriles as remote directing groups for palladium-catalyzed meta-selective C-H alkenylation and template-directed meta-selective C–H olefination of hydrocinnamic acid derivatives

기타 정보

Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product. Buyer assumes responsibility to confirm product identity and/or purity. All sales are final.

NOTWITHSTANDING ANY CONTRARY PROVISION CONTAINED IN SIGMA-ALDRICH′S STANDARD TERMS AND CONDITIONS OF SALE OR AN AGREEMENT BETWEEN SIGMA-ALDRICH AND BUYER, SIGMA-ALDRICH SELLS THIS PRODUCT "AS-IS" AND MAKES NO REPRESENTATION OR WARRANTY WHATSOEVER WITH RESPECT TO THIS PRODUCT, INCLUDING ANY (A) WARRANTY OF MERCHANTABILITY; (B) WARRANTY OF FITNESS FOR A PARTICULAR PURPOSE; OR (C) WARRANTY AGAINST INFRINGEMENT OF INTELLECTUAL PROPERTY RIGHTS OF A THIRD PARTY; WHETHER ARISING BY LAW, COURSE OF DEALING, COURSE OF PERFORMANCE, USAGE OF TRADE OR OTHERWISE.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


시험 성적서(COA)

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문서 라이브러리 방문

Dasheng Leow et al.
Nature, 486(7404), 518-522 (2012-06-29)
Functionalization of unactivated carbon-hydrogen (C-H) single bonds is an efficient strategy for rapid generation of complex molecules from simpler ones. However, it is difficult to achieve selectivity when multiple inequivalent C-H bonds are present in the target molecule. The usual

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