41036-32-2 Usage
Description
H-D-ALA-OBZL P-TOSYLATE, a benzoxazine derivative, is a chemical compound with potential applications in various fields due to its unique properties. It is characterized as a yellowish oil, which may suggest its potential use in certain industries or applications.
Uses
Used in Pharmaceutical Industry:
H-D-ALA-OBZL P-TOSYLATE is used as a modulator of chemokine receptors for the treatment of inflammatory and immunoregulatory diseases. Its role in modulating these receptors can help in managing and treating various conditions related to inflammation and immune system regulation.
Used in Chemical Industry:
Given its classification as a benzoxazine derivative and its physical state as a yellowish oil, H-D-ALA-OBZL P-TOSYLATE may also find applications in the chemical industry for various purposes, such as a reactant, intermediate, or additive in the synthesis of other compounds or materials. Its specific use would depend on the requirements of the chemical process and the desired outcome.
Check Digit Verification of cas no
The CAS Registry Mumber 41036-32-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,0,3 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 41036-32:
(7*4)+(6*1)+(5*0)+(4*3)+(3*6)+(2*3)+(1*2)=72
72 % 10 = 2
So 41036-32-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO2.C7H8O3S/c1-8(11)10(12)13-7-9-5-3-2-4-6-9;1-6-2-4-7(5-3-6)11(8,9)10/h2-6,8H,7,11H2,1H3;2-5H,1H3,(H,8,9,10)/t8-;/m1./s1
41036-32-2Relevant articles and documents
Mortiamides A-D, Cyclic Heptapeptides from a Novel Mortierella sp. Obtained from Frobisher Bay
Grunwald, Alyssa L.,Berrue, Fabrice,Robertson, Andrew W.,Overy, David P.,Kerr, Russell G.
supporting information, p. 2677 - 2683 (2017/11/06)
Four new cyclic heptapeptides, mortiamides A-D (1-4), were obtained from a novel Mortierella sp. isolate obtained from marine sediment collected from the intertidal zone of Frobisher Bay, Nunavut, Canada. The structures of the compounds were elucidated by NMR spectroscopy and tandem mass spectrometry. The absolute configurations of the amino acids were determined using Marfey's method. Localization of l and d amino acids within each compound was ascertained by retention time comparison of the partial hydrosylate products of each compound to synthesized dipeptide standards using LC-HRMS. Compounds 1-4 did not exhibit any significant antimicrobial or cytotoxic activity.