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908094-04-2

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908094-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 908094-04-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,8,0,9 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 908094-04:
(8*9)+(7*0)+(6*8)+(5*0)+(4*9)+(3*4)+(2*0)+(1*4)=172
172 % 10 = 2
So 908094-04-2 is a valid CAS Registry Number.

908094-04-2Relevant articles and documents

Complexes of [(dadi)Ti(L/X)]m That Reveal Redox Non-Innocence and a Stepwise Carbene Insertion into a Carbon-Carbon Bond

Heins, Spencer P.,Morris, Wesley D.,Cundari, Thomas R.,MacMillan, Samantha N.,Lobkovsky, Emil B.,Livezey, Nicholas M.,Wolczanski, Peter T.

, p. 3488 - 3501 (2018)

The addition of donors to (dadi)Ti(THF) (1-THF, dadi = [{-CH=N(1,2-C6H4)N(2,6-iPr2-C6H3)}2]n) afforded the adducts [(dadi)Ti(L/X)]m (1-L, m = 0, N2CPh2; m = -1, X = Cl-, N3-, OiPr-, CH3-, neoPe-, CH=CH2-, CCPh-, CCTMS-, H(D)-). In all adducts, the chelate was in the (dadi)4- redox state. For certain anions, evidence for intimate binding of the Li+ counterion was explored spectroscopically. Treatment of 1-THF with PhHCN2, yielded {PhC3H3(-NC6H4-2-NAr)2}Ti(THF) (3, Ar = 2,6-iPr2-C6H3), which contains a cyclopropanated dadi ligand. The mechanism was explored by calculations, and the addition of Ph2CN2 to 3 produced a nacnac derivative, {PhC(CHNC6H4-2-NAr)2}Ti(??2-HNNCPh2) (4, Ar = 2,6-iPr2-C6H3), generated via hydrogen transfer from the cyclopropane.

Cyclopropane compound as well as preparation method and application thereof

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Paragraph 0056; 0066-0068, (2017/08/19)

The invention discloses a cyclopropane compound as well as a preparation method and application thereof. The cyclopropane compound has a structure shown as formula I. The cyclopropane compound is prepared by taking a diazo compound and unsaturated ketone

PROCESS FOR THE CYCLOADDITION OF A HETERO(ARYL) 1,3-DIPOLE COMPOUND WITH A (HETERO)CYCLOALKYNE

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Paragraph 0415, (2017/01/26)

A process is provided, comprising reacting a (hetero)aryl 1,3-dipole compound with a (hetero)cycloalkyne, wherein the (hetero)aryl 1,3-dipole compound comprises a 1,3-dipole functional group bonded to a (hetero)aryl group, and wherein the (hetero)aryl 1,3-dipole compound is a (hetero)aryl azide or a (hetero)aryl diazo compound; wherein: (i) the (hetero)aryl group of the (hetero)aryl 1,3-dipole compound comprises a substituent (ii) the (hetero)aryl group of the (hetero)aryl 1,3-dipole compound is an electron-poor (hetero)aryl group and wherein the (hetero)cycloalkyne is a (hetero)cyclooctyne or a (hetero)cyclononyne according to Formula (1). The invention also relates to the products obtainable by the process according to the invention.

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