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169310-73-0

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169310-73-0 Usage

Uses

1-Methoxy-4-[(3-methyl-3-buten-1-yl)oxy]benzene is an intermediate in the synthesis of L-Isomer of Mevalonic acid (M339020), a precursor in the biosynthesis of cholesterol (C432501).

Check Digit Verification of cas no

The CAS Registry Mumber 169310-73-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,3,1 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 169310-73:
(8*1)+(7*6)+(6*9)+(5*3)+(4*1)+(3*0)+(2*7)+(1*3)=140
140 % 10 = 0
So 169310-73-0 is a valid CAS Registry Number.

169310-73-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methoxy-4-(3-methylbut-3-enoxy)benzene

1.2 Other means of identification

Product number -
Other names 1-methoxy-4-[(3-methylbut-3-en-1-yl)oxy]benzene

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:169310-73-0 SDS

169310-73-0Relevant articles and documents

PROTEIN TYROSINE PHOSPHATASE INHIBITORS AND METHODS OF USE THEREOF

-

Page/Page column 360, (2021/06/26)

Provided herein are compounds, compositions, and methods useful for inhibiting protein tyrosine phosphatase, e.g, protein tyrosine phosphatase non-receptor type 2 (PTPN2) and/or protein tyrosine phosphatase non-receptor type 1 (PTPN1), and for treating related diseases, disorders and conditions favorably responsive to PTPN1 or PTPN2 inhibitor treatment, e.g, a cancer or a metabolic disease.

7-Substituted 2-Nitro-5,6-dihydroimidazo[2,1-b][1,3]oxazines: Novel Antitubercular Agents Lead to a New Preclinical Candidate for Visceral Leishmaniasis

Thompson, Andrew M.,O’Connor, Patrick D.,Marshall, Andrew J.,Yardley, Vanessa,Maes, Louis,Gupta, Suman,Launay, Delphine,Braillard, Stephanie,Chatelain, Eric,Franzblau, Scott G.,Wan, Baojie,Wang, Yuehong,Ma, Zhenkun,Cooper, Christopher B.,Denny, William A.

supporting information, p. 4212 - 4233 (2017/06/05)

Within a backup program for the clinical investigational agent pretomanid (PA-824), scaffold hopping from delamanid inspired the discovery of a novel class of potent antitubercular agents that unexpectedly possessed notable utility against the kinetoplast

A Ring-Closing Enyne Metathesis Approach to Functionalized Semicyclic Dienes: The Total Synthesis of (-)-Tetrangomycin

Moodie, Lindon W. K.,Larsen, David S.

, p. 1684 - 1694 (2015/10/05)

The angucycline antibiotic (-)-tetrangomycin was synthesized in 13 steps (11 % overall yield) by using a stereoselective Diels-Alder reaction between a naphthoquinone and a semicyclic diene to construct the benz[a]anthraquinone ring system. The diene inte

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