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(2S,4S,5S)-4-hydroxymethyl-2-phenyl-5-(2-propenyl)-1,3-dioxacyclohexane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

135840-16-3

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135840-16-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135840-16-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,8,4 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 135840-16:
(8*1)+(7*3)+(6*5)+(5*8)+(4*4)+(3*0)+(2*1)+(1*6)=123
123 % 10 = 3
So 135840-16-3 is a valid CAS Registry Number.

135840-16-3Downstream Products

135840-16-3Relevant academic research and scientific papers

E-Selectin Antagonists Modified By Macrocycle Formation to the Galactose

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Paragraph 0301, (2016/12/07)

Provided herein are glycomimetic E-selectin antagonist compounds of formula (I)) and pharmaceutical compositions comprising at least one of the same. The compounds of the present disclosure include trisaccharide domain mimics comprising at least one macro

E-SELECTIN ANTAGONISTS MODIFIED BY MACROCYCLE FORMATION TO THE GALACTOSE

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Paragraph 00215, (2015/08/03)

Provided herein are glycomimetic E-selectin antagonist compounds of formula (I)) and pharmaceutical compositions comprising at least one of the same. The compounds of the present disclosure include trisaccharide domain mimics comprising at least one macro

Stereocontrolled synthesis of C10-C22 fragment of the immunosuppressant FK 506. An occurrence of complementary stereoselectivity in the C15 ketone reduction

Morimoto, Yoshiki,Mikami, Atsushi,Kuwabe, Shin-Itsu,Shirahama, Haruhisa

, p. 3371 - 3390 (2007/10/03)

The stereoselective syntheses of the C10-C22 fragment 2a and its C15-epimer 2b of the immunosuppressant FK 506 1 have been carried out through convergent coupling of the sulfone 3, which could be constructed by highly stereocontrolled ester-enolate Claise

A Synthesis of C1-C22 Fragment of the Immunosuppressant FK 506. Stereoselective Construction of (E)-Trisubstituted Double Bond (C19-C20) via Ester-enolate Claisen Rearrangement

Morimoto, Yoshiki,Mikami, Atsushi,Kuwabe, Shin-itsu,Shirahama, Haruhisa

, p. 2909 - 2912 (2007/10/02)

An ene-ester 5 prepared from L-malic acid was subjected to the ester-enolate Claisen rearrangement under Ireland's condition to give stereoselectively C16-C22 fragment 11 containing (E)-trisubstituted double bond which was further advanced to C1-C22 fragm

Enantiomerically Pure Building Blocks for Syntheses from Branched Malates

Aebi, Johannes D.,Sutter, Marius A.,Wasmuth, Daniel,Seebach, Dieter

, p. 2114 - 2126 (2007/10/02)

Isocitric acid lactone (13) and the chiral building blocks (2S,3R)-4-bromo-1,2-epoxy-3-methyl-butane (21), cis- and trans 2,3-epoxy-2-methylsuccinates (23, 24), and the singly protected (2R)-2-methyl-, -2-allyl- and -2-benzyl-1,3-propanediols (32a, b, c)

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