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15(S)-15-METHYL PROSTAGLANDIN D2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85280-90-6

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85280-90-6 Usage

Uses

15(S)-15-methyl Prostaglandin D2 is a synthetic analog of PGD2.

Check Digit Verification of cas no

The CAS Registry Mumber 85280-90-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,2,8 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 85280-90:
(7*8)+(6*5)+(5*2)+(4*8)+(3*0)+(2*9)+(1*0)=146
146 % 10 = 6
So 85280-90-6 is a valid CAS Registry Number.
InChI:InChI=1/C21H34O5/c1-3-4-9-13-21(2,26)14-12-17-16(18(22)15-19(17)23)10-7-5-6-8-11-20(24)25/h5,7,12,14,16-18,22,26H,3-4,6,8-11,13,15H2,1-2H3,(H,24,25)/b7-5-,14-12+/t16-,17-,18+,21+/m1/s1

85280-90-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 15(S)-15-methyl Prostaglandin D2

1.2 Other means of identification

Product number -
Other names 15s)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:85280-90-6 SDS

85280-90-6Downstream Products

85280-90-6Relevant academic research and scientific papers

Enantio- and stereospecific syntheses of 15(R)-Me-PGD2, a potent and selective DP2-receptor agonist

Patel, Pranav,Lee, Gue-Jae,Kim, Seongjin,Grant, Gail E.,Powell, William S.,Rokach, Joshua

supporting information; body text, p. 7213 - 7218 (2009/05/26)

(Chemical Equation Presented) The first total synthesis of 15(R)-Me-PGD2 3 is reported. The synthesis is based on the enantioselective and stereospecific syntheses of synthon 17 and its attachment to the five-membered ring by a olefin cross metathesis reaction. This approach permits the introduction of a side chain with a predetermined stereogenic center into the prostanoid ring, resulting in the synthesis of 15R-methyl prostaglandin D2 and allows rapid access to other prostanoids.

Synthesis and Platelet Aggregation Inhibiting Activity of Prostaglandin D Analogues

Bundy, Gordon L.,Morton, D. R.,Peterson, D. C.,Nishizawa, E. E.,Miller, W. L.

, p. 790 - 799 (2007/10/02)

Several prostaglandin D (PGD) analogues have been synthesized, incorpotating the following variations: (a) varying degrees of side-chain unsaturation, (b) C-9 hydroxy removed or in the unnatural 9β configuration, (c) metabolically stabilized analogues (e.

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