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(2S,3R)-methyl 2-(4-(benzyloxy)phenyl)-5-bromo-2,3-dihydrobenzofuran-3-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

616898-40-9

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616898-40-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 616898-40-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,6,8,9 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 616898-40:
(8*6)+(7*1)+(6*6)+(5*8)+(4*9)+(3*8)+(2*4)+(1*0)=199
199 % 10 = 9
So 616898-40-9 is a valid CAS Registry Number.

616898-40-9Relevant academic research and scientific papers

Dirhodium tetracarboxylate derived from adamantylglycine as a chiral catalyst for carbenoid reactions

Reddy, Ravisekhara P.,Lee, Gene H.,Davies, Huw M. L.

, p. 3437 - 3440 (2006)

The dirhodium tetracarboxylate, Rh2(S-PTAD)4, derived from adamantylglycine, is a very effective chiral catalyst for carbenoid reactions. High asymmetric induction was obtained in Rh2(S-PTAD) 4-catalyzed intramo

COMPOUND, ALPHA 1 ADRENALINE RECEPTOR ANTAGONIST, AND COMPOSITION

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Page/Page column 17; 26, (2009/12/23)

A novel compound, a novel α1 adrenergic receptor antagonistic agent, and a novel composition are provided which are capable of exerting a therapeutic effect on treatment of hypertension as well as treatment of prostatic hypertrophy and the like. The compound is represented by the following formula (1):

Catalysts for use in enantioselective synthesis

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Page/Page column 44; 52, (2008/12/05)

Disclosed are compounds having the following formula: in which Z11 is selected from a substituted or unsubstituted saturated adamantyl or other polycyclic group and a substituted or unsubstituted branched acyclic group containing at least 5 carbon atoms at least one of which is a tertiary carbon; and in which Z12 is a cyclic imide. Methods of using these compounds as chiral catalysts for carbenoid reactions and for enantioselective C—H aminations are also described.

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