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Benzene, 1,2-dimethoxy-4-(1-methylethoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77106-50-4

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77106-50-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77106-50-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,0 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 77106-50:
(7*7)+(6*7)+(5*1)+(4*0)+(3*6)+(2*5)+(1*0)=124
124 % 10 = 4
So 77106-50-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H16O3/c1-8(2)14-9-5-6-10(12-3)11(7-9)13-4/h5-8H,1-4H3

77106-50-4SDS

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 1,2-dimethoxy-4-propan-2-yloxybenzene

1.2 Other means of identification

Product number -
Other names 3,4-Dimethoxy-1-isopropoxybenzene

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:77106-50-4 SDS

77106-50-4Relevant academic research and scientific papers

First total synthesis of medicinally important 3,4,7-trimethoxy-9,10-dihydrophenanthrene-1,5-diol

Gangireddy Venkata, Sivarami Reddy,Narkhede, Umesh C.,Jadhav, Vinod D.,Gangu Naidu, Ch.

, p. 1670 - 1673 (2018/03/29)

The first total synthesis was successfully achieved for biologically active 9,10-dihydrophenanthrene-1,5-diol. The key features of our synthetic approach are Perkin condensation, followed by bromination, palladium mediated intramolecular C-C bond coupling, and selective isopropyl ether cleavage. Synthesized compounds were purified and characterized by IR, 1HNMR, 13CNMR and HRMS/LC-MS.

Synthesis of Lamellarin G Trimethyl Ether by von Miller–Pl?chl-Type Cyclocondensation

Colligs, Vanessa C.,Dialer, Clemens,Opatz, Till

, p. 4064 - 4070 (2018/07/31)

A concise synthesis of lamellarin G trimethyl ether based on a von Miller–Pl?chl-type cyclocondensation of a deprotonated α-amino nitrile with an α,β-unsaturated ketone as the key step was developed. The general strategy does not rely on molecular symmetry and allows for the independent variation of the substitution pattern.

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