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123186-35-6

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123186-35-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123186-35-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,1,8 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 123186-35:
(8*1)+(7*2)+(6*3)+(5*1)+(4*8)+(3*6)+(2*3)+(1*5)=106
106 % 10 = 6
So 123186-35-6 is a valid CAS Registry Number.

123186-35-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(hex-5-ynoxymethyl)-4-methoxybenzene

1.2 Other means of identification

Product number -
Other names Benzene,1-[(5-hexynyloxy)methyl]-4-methoxy

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:123186-35-6 SDS

123186-35-6Relevant articles and documents

Dictating Thermodynamic Control through Tethering: Applications to Stereoselective Bis-Spiroketal Synthesis

Asari, Austin H.,Floreancig, Paul E.

, p. 6622 - 6626 (2020)

Approaches to stereocontrol that invoke thermodynamic control fail when two or more potential products are energetically similar, but rational structural perturbations can be employed to break the energetic degeneracy and provide selective transformations. This manuscript illustrates that tethering is an effective approach for the stereoselective construction of bis-spiroketals with thermodynamically similar stereoisomers, providing a new approach to set remote stereocenters and prepare complex structures that have not previously been accessed stereoselectively.

SYNTHESIS OF DELTA 12-PGJ3 AND RELATED COMPOUNDS

-

Page/Page column 133, (2015/04/15)

In one aspect, the present invention provides novel derivatives of Δ12-PGJ3 and modular synthetic pathways to obtaining Δ12-PGJ3 and derivatives thereof. In some aspects, the present derivatives of Δ12-PGJ3 are useful as chemotherapeutic agents. The present disclosure also describes compositions of these derivatives as well as methods of use of the derivatives thereof.

Sustainable, mild and efficient p-methoxybenzyl ether deprotections utilizing catalytic DDQ

Walsh, Katie,Sneddon, Helen F.,Moody, Christopher J.

, p. 7380 - 7387 (2017/09/13)

A procedure for the selective deprotection of p-methoxybenzyl ethers using catalytic amounts of DDQ and of sodium nitrite, with oxygen as the terminal oxidant, is reported.

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