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(3S)-tert-butyl 3-benzyl-3-[(1R)-2-nitro-1-phenylethyl]-2-oxoindoline-1-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1333342-48-5

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1333342-48-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1333342-48-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,3,3,4 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1333342-48:
(9*1)+(8*3)+(7*3)+(6*3)+(5*3)+(4*4)+(3*2)+(2*4)+(1*8)=125
125 % 10 = 5
So 1333342-48-5 is a valid CAS Registry Number.

1333342-48-5Downstream Products

1333342-48-5Relevant academic research and scientific papers

Michael addition of N-unprotected 2-oxindoles to nitrostyrene catalyzed by bifunctional tertiary amines: Crucial role of dispersion interactions

Reiter, Christoph,Lopez-Molina, Sonia,Schmid, Bernhard,Neiss, Christian,Goerling, Andreas,Tsogoeva, Svetlana B.

, p. 1324 - 1332 (2014/05/20)

Bifunctional thiourea- or sulfonamide-derived tertiary amines catalyze the enantioselective nitro-Michael addition of N-unprotected 3-substituted 2-oxindoles to nitrostyrene in up to 99 % yields, 94:6 er, and 87:13 dr. Overcoming the necessity to introduc

Novel tartrate-derived guanidine-catalyzed highly enantio- and diastereoselective Michael addition of 3-substituted oxindoles to nitroolefins

Zou, Liwei,Bao, Xiaoze,Ma, Yuanyuan,Song, Yuming,Qu, Jingping,Wang, Baomin

supporting information, p. 5760 - 5762 (2014/05/20)

The Michael addition of 3-substituted oxindoles to nitroolefins was catalyzed by a novel tartrate-derived guanidine in high yield with excellent diastereo- and enantioselectivity. This method showed an extraordinarily broad substrate scope in terms of both reaction partners. the Partner Organisations 2014.

Squaramide-catalyzed diastereo- and enantioselective Michael addition of 3-substituted oxindoles to nitroalkenes

Yang, Wen,Wang, Jingsi,Du, Da-Ming

experimental part, p. 972 - 980 (2012/09/22)

An efficient diastereo- and enantioselective Michael addition of 3-substituted oxindoles onto nitroalkenes catalyzed by a bifunctional chiral squaramide catalyst has been developed. This organocatalytic reaction with 2 mol % of catalyst proceeded smoothly

Asymmetric michael addition of N-Boc-protected oxindoles to nitroalkenes catalyzed by a chiral secondary amine

Wang, Chuan,Yang, Xuena,Enders, Dieter

supporting information; experimental part, p. 4832 - 4835 (2012/05/20)

New mission for prolinol ethers: A secondary-amine-catalyzed Michael addition of N-Boc-protected oxindoles to nitroalkenes through a Bronsted base activation mode has been developed, furnishing the products in excellent yields (88-98%), diastereoselectivi

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