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2-(2-(1,3-dioxan-2-yl)-6-(methoxymethoxy)-4-methylphenyl)-5-hydroxynaphthalene-1,4-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1262052-77-6

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1262052-77-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1262052-77-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,2,0,5 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1262052-77:
(9*1)+(8*2)+(7*6)+(6*2)+(5*0)+(4*5)+(3*2)+(2*7)+(1*7)=126
126 % 10 = 6
So 1262052-77-6 is a valid CAS Registry Number.

1262052-77-6Relevant articles and documents

Total synthesis of jadomycins B, S, T, and ILEVS1080

Yang, Xiaoyu,Yu, Biao

, p. 8431 - 8434 (2013)

Sweetening up jadomycin A: The first total synthesis of jadomycins B, S, T, and ILEVS1080 has been achieved, featuring construction of the unique 8H-benz[b]oxazolo[3,3-f]phenanthridine skeleton by biomimetic condensation of a quinone aldehyde with amino acid sodium salts and elaboration of the glycosides by Mitsunobu condensation (see figure). Copyright

Roles of the synergistic reductive O-methyltransferase GilM and of O-methyltransferase GilMT in the gilvocarcin biosynthetic pathway

Tibrewal, Nidhi,Downey, Theresa E.,Van Lanen, Steven G.,Ul Sharif, Ehesan,O'Doherty, George A.,Rohr, Juergen

experimental part, p. 12402 - 12405 (2012/09/05)

Two enzymes of the gilvocarcin biosynthetic pathway, GilMT and GilM, with unclear functions were investigated by in vitro studies using purified, recombinant enzymes along with synthetically prepared intermediates. The studies revealed GilMT as a typical

Total synthesis of jadomycin A and a carbasugar analogue of jadomycin B

Shan, Mingde,Sharif, Ehesan U.,O'Doherty, George A.

supporting information; experimental part, p. 9492 - 9495 (2011/02/22)

One's trash is another one's treasure: The first syntheses of jadomycin A and the carbasugar analogue of jadomycin B have been achieved in 6 and 20 longest linear steps, respectively. The key ring system of the aglycone was prepared by a 6π-electron elect

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