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10375-46-9

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10375-46-9 Usage

Physical state

Yellow crystalline compound

Usage

Yellow pigment in organic synthesis and coordination chemistry

Application

Formation of metal complexes as a ligand

Application

Synthesis of chalcone derivatives

Application

Formation of chiral iminophosphines

Property

Ability to form stable complexes with a wide range of metal ions

Importance

Valuable tool in the study of metal coordination chemistry

Versatility

Important applications in various fields of chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 10375-46-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,7 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10375-46:
(7*1)+(6*0)+(5*3)+(4*7)+(3*5)+(2*4)+(1*6)=79
79 % 10 = 9
So 10375-46-9 is a valid CAS Registry Number.

10375-46-9Downstream Products

10375-46-9Relevant articles and documents

Highly efficient addition of activated methylene compounds to alkenes catalyzed by gold and silver

Yao, Xiaoquan,Li, Chao-Jun

, p. 6884 - 6885 (2004)

A highly efficient intermolecular addition of 1,3-diketones to alkenes catalyzed by AuCl3/AgOTf was developed. A mechanistic rationale for the reaction has been proposed via a α-C-H activation. Copyright

Solvent-free alkylation of 1,3-dicarbonyl compounds with benzylic, propargylic and allylic alcohols catalyzed by La(NO3)3·6H2O

Subramanyam, Madala,Rao, Koya Prabhakara,Varala, Ravi,Rao, Mandava V. Basaveswara

, p. 1155 - 1160 (2016/03/01)

An efficient and solvent free method for benzylation, propargylation and allylation of 1,3-dicarbonyl compounds with alcohols has been developed by using La(NO3)3·6H2O as water tolerable catalyst. The reaction was shown to proceed smoothly for various 1,3-dicarbonyl compounds with benzylic, propargylic and allylic alcohols including 1° allylic alcohols, without any solvent, providing a clean access to the desired products in short reaction times with good to excellent yields and high selectivity.

Heteropoly acid-catalyzed highly efficient alkylation of 1,3-dicarbonyl compounds with benzylic and propargylic alcohols

Yadav,Subba Reddy,Pandurangam,Raghavendra Rao,Praneeth,Narayana Kumar,Madavi,Kunwar

, p. 4296 - 4301 (2008/09/21)

Various 1,3-dicarbonyl compounds reacted readily with benzylic and propargylic alcohols in the presence of 10 mol % of phosphomolybdic acid supported on silica gel (PMA/SiO2) under mild reaction conditions to produce 2-benzylic- and 2-propargyl

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