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2H-Pyran-2-one, tetrahydro-4-(methoxymethoxy)-6-[3-[(4-methoxyphenyl)methoxy]propyl]- 3,5-dimethyl-, (3R,4S,5R,6S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

565229-05-2

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  • 2H-Pyran-2-one, tetrahydro-4-(methoxymethoxy)-6-[3-[(4-methoxyphenyl)methoxy]propyl]- 3,5-dimethyl-, (3R,4S,5R,6S)-

    Cas No: 565229-05-2

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  • 2H-Pyran-2-one, tetrahydro-4-(methoxymethoxy)-6-[3-[(4-methoxyphenyl)methoxy]propyl]- 3,5-dimethyl-, (3R,4S,5R,6S)-

    Cas No: 565229-05-2

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  • Weiyel Inc
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565229-05-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 565229-05-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,5,2,2 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 565229-05:
(8*5)+(7*6)+(6*5)+(5*2)+(4*2)+(3*9)+(2*0)+(1*5)=162
162 % 10 = 2
So 565229-05-2 is a valid CAS Registry Number.

565229-05-2Downstream Products

565229-05-2Relevant articles and documents

ANALOGS OF DISCODERMOLIDE AND DICTYOSTATIN-1, INTERMEDIATES THEREFOR AND METHODS OF SYNTHESIS THEREOF

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Page 35-36, (2008/06/13)

A compound of the following structure: wherein R1 is H, an alkyl group, an aryl group, an alkenyl group, an alkynyl group, or a halogen atom; R2 is H, an alkyl group, an aryl group, a benzyl group, a trityl group, -SiRaRbRc, CH2ORd, or CORe; Ra, Rb and Rc are independently an alkyl group or an aryl group; Rd is an alkyl group, an aryl group, an alkoxylalkyl group, -RiSiRaRbRc or a benzyl group, wherein Ri is an alkylene group; Re is an alkyl group, an allyl group, a benzyl group, an aryl group, an alkoxy group, or -NRgRh, wherein Rg and Rh are independently H, an alkyl group or an aryl group; R3 is (CH2)n where n is and integer in the range of 0 to 5, -CH2CH(CH3)-, -CH=CH-, -CH=C(CH3)-, or -C=-C-; R4 is (CH2)p where p is an integer in the range of 4 to 12, -(CHRkl)yl (CHRk2)y2(CHRk3)y3(CHRk4)y4(CHRk5)y5C(Rsl )=C(Rs2)C(Rs3)=C(Rs4)-, -(CHRk1 )yl (CHRk2)y2(CHRk3)y3(CHRk4)y4(CHRk5)y5CH(RsI)CH(Rs2)C(Rs3)=C(Rs4)-, -(CHRk1)yl (CHRk2)y2(CHRk3)y3(CHRk4)y4(CHRks)y5C(Rsl)=C(Rs2)CH(Rs3)CH(Rs4)-, -(CHRkI )yl (CHRk2)y2(CHRk3)y3(CHRk4)y4(CHRk5)y5CH(Rsl)CH(Rs2)CH(Rs3)CH(R s4)-,wherein y1 and y2 are 1 and y3, y4 and y5 are independently 0 or 1, Rk1, Rk2, Rk3, Rk4 and Rk5 are independently H, CH3, or OR2a, and Rs1,Rs2, Rs3, and Rs4 are independently H or CH3, wherein R2a is H, an alkyl group, an aryl group, a benzyl group, a trityl group, -SiRaRbRc, CH2ORd, or CORe; and R5 is H or OR2b, wherein R2b is H, an alkyl group, an aryl group, an aryl group, a benzyl group, a trityl group, -SiRaRbRc, CH2ORd, or CORe; provided that the compound is not dictyostatin 1.

Simplified discodermolide analogues: Synthesis and biological evaluation of 4-epi-7-dehydroxy-14,16-didemethyl-(+)-discodermolides as microtubule-stabilizing agents

Choy, Nakyen,Shin, Youseung,Nguyen, Phu Qui,Curran, Dennis P.,Balachandran, Raghavan,Madiraju, Charitha,Day, Billy W.

, p. 2846 - 2864 (2007/10/03)

Several novel analogues of (+)-discodermolide were synthesized via a convergent strategy that used Wittig reactions to append left and right side chains to a central scaffold and then tested for biological activity. Three of the analogues in the 4-epi-7-d

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