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Phenyl-acetic acid (3R,4S,5S,6R,7R,9R,11R,12R,13S,14R)-6-((2S,3R,4S,6R)-3-acetoxy-4-dimethylamino-6-methyl-tetrahydro-pyran-2-yloxy)-14-ethyl-12,13-dihydroxy-7-methoxy-3,5,7,9,11,13-hexamethyl-2,10-dioxo-oxacyclotetradec-4-yl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

382606-10-2

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382606-10-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 382606-10-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,2,6,0 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 382606-10:
(8*3)+(7*8)+(6*2)+(5*6)+(4*0)+(3*6)+(2*1)+(1*0)=142
142 % 10 = 2
So 382606-10-2 is a valid CAS Registry Number.

382606-10-2Downstream Products

382606-10-2Relevant academic research and scientific papers

Synthesis and antibacterial activity of a novel series of acylides: 3-O-(3-pyridyl)acetylerythromycin A derivatives

Tanikawa, Tetsuya,Asaka, Toshifumi,Kashimura, Masato,Suzuki, Keiko,Sugiyama, Hiroyuki,Sato, Masakazu,Kameo, Kazuya,Morimoto, Shigeo,Nishida, Atsushi

, p. 2706 - 2715 (2003)

A novel series of acylides, 3-O-(aryl)acetylerythromycin A derivatives, were synthesized and evaluated. These compounds have significant potent antibacterial activity against not only Gram-positive pathogens, including inducibly macrolide-lincosamide-stre

Synthesis and antibacterial activity of acylides (3-O-acyl-erythromycin derivatives): A novel class of macrolide antibiotics

Tanikawa,Asaka,Kashimura,Misawa,Suzuki,Sato,Kameot,Morimoto,Nishida

, p. 4027 - 4030 (2007/10/03)

Introduction of an acyl group to the 3-O-position of erythromycin A derivatives instead of L-cladinose led to a novel class of macrolide antibiotics that we named "acylides". The 3-O-nitrophenylacetyl derivative TEA0777 showed significantly potent activit

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