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194805-14-6

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194805-14-6 Usage

General Description

"(1R)-5-Bromo-1-methyl-2-trityl-2,3-dihydro-1H-isoindole" is a chemical compound with a molecular formula C29H27BrN and a molecular weight of 456.43 g/mol. It is an isoindole derivative with a bromine atom and a methyl group attached to the carbon atoms. The compound also contains a trityl group, which is a bulky and aromatic protecting group often used in organic synthesis. (1R)-5-Bromo-1-methyl-2-trityl-2,3-dihydro-1H-isoindole may have potential applications in organic chemistry and pharmaceutical research, particularly in the development of novel chemical reactions and the synthesis of biologically active molecules. Its specific properties and potential uses in various fields may warrant further investigation and study.

Check Digit Verification of cas no

The CAS Registry Mumber 194805-14-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,8,0 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 194805-14:
(8*1)+(7*9)+(6*4)+(5*8)+(4*0)+(3*5)+(2*1)+(1*4)=156
156 % 10 = 6
So 194805-14-6 is a valid CAS Registry Number.
InChI:InChI=1/C28H24BrN/c1-21-27-18-17-26(29)19-22(27)20-30(21)28(23-11-5-2-6-12-23,24-13-7-3-8-14-24)25-15-9-4-10-16-25/h2-19,21H,20H2,1H3/t21-/m1/s1

194805-14-6Relevant articles and documents

Traceless Directing Group Assisted Cobalt-Catalyzed C?H Carbonylation of Benzylamines

Ling, Fei,Ai, Chongren,Lv, Yaping,Zhong, Weihui

, p. 3707 - 3712 (2017/10/07)

The first example of cobalt-catalyzed C(sp2)?H carbonylation of benzylamines using a traceless directing group is reported, which was successfully applied to the synthesis of N?unprotected iso-indolinones through direct C?H/N?H bonds activation. This protocol tolerates a variety of functional groups and provides a facile and efficient method for the formal synthesis of (+)-garenoxacin. (Figure presented.).

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