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(R)-N-benzyl-1-((3aR,5R,6S,6aR)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)prop-2-en-1-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

299409-50-0

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299409-50-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 299409-50-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,9,4,0 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 299409-50:
(8*2)+(7*9)+(6*9)+(5*4)+(4*0)+(3*9)+(2*5)+(1*0)=190
190 % 10 = 0
So 299409-50-0 is a valid CAS Registry Number.

299409-50-0Downstream Products

299409-50-0Relevant academic research and scientific papers

A short and common stereoselective approach to 5/6, 6/6, 6/7 bicyclic aza sugars

Chandrasekhar,Venkateswara Rao,Veera Mohana Rao,Jagadeesh

experimental part, p. 1217 - 1223 (2009/12/01)

An efficient and highly stereoselective approach to bicyclic aza sugars is described using Grignard reaction on an N-benzyl imine derived from 3-O-benzyl-1,2-O-isopropylidine-α-d-xylo-pentodialdofuranose, ring closing metathesis, and reductive cyclization

Synthesis of pentahydroxy indolizidine alkaloids using ring closing metathesis: Attempts to find the correct structure of uniflorine A

Karanjule, Narayan S.,Markad, Shankar D.,Dhavale, Dilip D.

, p. 6273 - 6276 (2007/10/03)

Ring closing metathesis of D-glucose derived diene-substrate containing nitrogen functionality followed by asymmetric dihydroxylation afforded sugar substituted dihydroxylated pyrrolidines 8a-c which on 1,2-acetonide deprotection and reductive amination a

Intramolecular 5-endo-trig aminomercuration of β-hydroxy-γ- alkenylamines: Efficient route to a pyrrolidine ring and its application for the synthesis of (+)-castanospermine and analogues

Karanjule, Narayan S.,Markad, Shankar D.,Shinde, Vaishali S.,Dhavale, Dilip D.

, p. 4667 - 4670 (2007/10/03)

The intramolecular aminomercuration reaction of sugar-derived β-hydroxy-γ-alkenylamines 8a-c undergoes 5-endo-trig cyclization in high yield. The sugar-substituted pyrrolidines thus obtained were elaborated to the synthesis of polyhydroxylated indolizidin

A general method for the vinylation of nitrones. Synthesis of allyl hydroxylamines and allyl amines

Merino, Pedro,Anoro, Sonia,Franco, Santiago,Gascon, Jose M.,Martin, Victor,Merchan, Francisco L.,Revuelta, Julia,Tejero, Tomas,Tunon, Victoria

, p. 2989 - 3021 (2007/10/03)

An examination of the vinylation of several nitrones is presented. Whereas a complete diastereofacial discrimination was observed upon the addition of vinyl organometallic reagents to α-alkoxy nitrones, the same reaction with α-amino nitrones gave syn add

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