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(S)-3-cyclohexyl-1,2-propanediol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

216088-17-4

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216088-17-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 216088-17-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,6,0,8 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 216088-17:
(8*2)+(7*1)+(6*6)+(5*0)+(4*8)+(3*8)+(2*1)+(1*7)=124
124 % 10 = 4
So 216088-17-4 is a valid CAS Registry Number.

216088-17-4Relevant academic research and scientific papers

Regioselective oxidative cleavage of benzylidene acetals: Synthesis of α- and β-benzoyloxy carboxylic acids

Kumar, Ponminor Senthil,Banerjee, Amit,Baskaran, Sundarababu

scheme or table, p. 804 - 807 (2010/04/06)

(Chemical Equation Presented) Ruthenium has twice the fun: The synthetic potential of the highly regio- and stereoselective title reaction, which relies on two oxidative cleavage steps promoted by RuCI3 in combination with NaIO 4 (see example; Bz = benzoyl), was demonstrated with the synthesis of biologically active cis-(2R,3S)-3-hydroxypipecolic acid from D-glucose.

Inhibitors of protein isoprenyl transferases

-

, (2008/06/13)

Compounds having the formula STR1or a pharmaceutically acceptable salt thereof wherein R 1 is (a) hydrogen, (b) loweralkyl, (c) alkenyl, (d) alkoxy, (e) thioalkoxy, (f) halo, (g) haloalkyl, (h) aryl-L 2 --, and (i) heterocyclic-L 2 --; R 2 is selected from STR2(b) --C(O)NH--CH(R 14)--C(O)OR 15, STR3(d) --C(O)NH--CH(R 14)--C(O)NHSO 2 R 16, (e) --C(O)NH--CH(R 14)-tetrazolyl, (f) --C(O)NH-heterocyclic, and (g) --C(O)NH--CH(R 14)--C(O)NR 17 R 18 ; R 3 is heterocyclic, aryl, substituted or unsubstituted cycloalkyl; R 4 is hydrogen, lower alkyl, haloalkyl, halogen, aryl, arylakyl, heterocyclic, or (heterocyclic)alkyl; L 1 is absent or is selected from (a) --L 4 --N(R 5)--L 5 --, (b) --L 4 --O--L 5 --, (c) --L 4 --S(O) n --L 5 -- (d) --L 4 --L 6 --C(W)--N(R 5)--L 5 --, (e) --L 4 --L 6 --S(O)m--N(R 5)--L 5 --, (f) --L 4 --N(R 5)--C(W)--L 7 --L 5 --, (g) --L 4 --N(R 5)--S(O) p --L 7 --L 5 --, (h) optionally substituted alkylene, (i) optionally substituted alkenylene, and (j) optionally substituted alkynylene are inhibitors of protein isoprenyl transferases. Also disclosed are protein isoprenyl transferase inhibiting compositions and a method of inhibiting protein isoprenyl transferases.

Inhibitors of protein isoprenyl transferases

-

, (2008/06/13)

The present invention relates to novel compounds of Formula I which are useful in inhibiting protein isoprenyl transferases and the farnesylation or geranylgeranylation of the oncogene protein Ras and other related small g-proteins, and compositions containing such compounds and methods of using such compounds.

A HIGHLY STEREOSELECTIVE CONVERSION OF α,β-EPOXY ESTERS TO α-HYDROXY ESTERS. AN EFFICIENT ROUTE TO OPTICALLY ACTIVE α-HYDROXYESTERS

Otsubo, Kenji,Inanaga, Junji,Yamaguchi, Masaru

, p. 4435 - 4436 (2007/10/02)

α,β-Epoxy esters were cleanly converted to α-hydroxy esters with retention of the configurations at the α-carbon atoms via MgI2-promoted regioselective oxirane ring-opening followed by tributyltin hydride-reduction.

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