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(3aR,4S,9aS)-N-phenyl-3,3a,4,9a-tetrahydro-2H-furo[2,3-b]chromen-4-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1264749-03-2

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1264749-03-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1264749-03-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,4,7,4 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1264749-03:
(9*1)+(8*2)+(7*6)+(6*4)+(5*7)+(4*4)+(3*9)+(2*0)+(1*3)=172
172 % 10 = 2
So 1264749-03-2 is a valid CAS Registry Number.

1264749-03-2Downstream Products

1264749-03-2Relevant articles and documents

Br?nsted acids of anionic chiral Co(III) complexes as catalysts for the stereoselective synthesis of cis-4-aminofuranobenzopyrans

Jiang, Hua-Jie,Liu, Kun,Wang, Jing,Li, Na,Yu, Jie

supporting information, p. 9077 - 9080 (2017/11/14)

A highly enantioselective interrupted Povarov reaction of salicylaldimines and 2,3-dihydrofuran was developed, through the elegant Br?nsted acid catalysis of anionic chiral Co(iii) complexes. This reaction affords the cis-4-aminofuranobenzopyran derivativ

Asymmetric synthesis of cis-4-aminobenzopyran derivatives catalyzed by N,N′-Dioxide-Sc(OTf)3 complexes

Zhang, Yulong,Dong, Shunxi,Liu, Xiaohua,Xie, Mingsheng,Zhu, Yin,Lin, Lili,Feng, Xiaoming

supporting information; experimental part, p. 13684 - 13687 (2012/02/01)

The reactions of salicylaldimines with electron-rich alkenes (2,3-dihydro-2H-furan and 3,4-dihydro-2H-pyran) catalyzed by N,N′-dioxide-Sc(OTf)3 complexes were investigated. The methodology was successfully applied to the asymmetric synthesis of

Catalytic asymmetric inverse-electron-demand (IED) [4+2] cycloaddition of salicylaldimines: Preparation of optically active 4-aminobenzopyran derivatives

Bernardi, Luca,Comes-Franchini, Mauro,Fochi, Mariafrancesca,Leo, Virginia,Mazzanti, Andrea,Ricci, Alfredo

supporting information; experimental part, p. 3399 - 3406 (2011/02/23)

The catalytic asymmetric inverse-electron-demand (IED) [4+2] cycloaddition of various salicylaldehyde-derived N-arylimines with electron-rich alkenes in the presence of chiral BINOL-derived phosphoric acid catalysts has been studied with the aim of obtaining optically active 4-aminobenzopyran derivatives. Dienophiles such as 2,3-dihydro-2H-furan, benzyl N-vinylcarbamate and 2-vinylindole have been employed. Copyright

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