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2,5-Cyclohexadiene-1-carboxylic acid, 1-(methoxymethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65984-94-3

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65984-94-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65984-94-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,9,8 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 65984-94:
(7*6)+(6*5)+(5*9)+(4*8)+(3*4)+(2*9)+(1*4)=183
183 % 10 = 3
So 65984-94-3 is a valid CAS Registry Number.

65984-94-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(methoxymethyl)cyclohexa-2,5-diene-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2,5-Cyclohexadiene-1-carboxylic acid,1-(methoxymethyl)

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:65984-94-3 SDS

65984-94-3Relevant academic research and scientific papers

Catalytic Enantioselective Birch–Heck Sequence for the Synthesis of Phenanthridinone Derivatives with an All-Carbon Quaternary Stereocenter

Sexton, Mary,Malachowski, William P.,Yap, Glenn P. A.,Rachii, Diana,Feldman, Greg,Krasley, Andrew T.,Chen, Zhilin,Tran, My Anh,Wiley, Kalyn,Matei, Alexandra,Petersen, Samantha,Tien, Sabrina Tran

, p. 1154 - 1172 (2022/01/20)

Novel phenanthridinone analogues with an all-carbon quaternary stereocenter have been enantioselectively synthesized using the Birch–Heck sequence. Flat phenanthridinone structures have extensive bioactivity but consequently also suffer from poor therapeutic selectivity. The addition of a quaternary center to the phenanthridinone skeleton has the potential to generate more complex analogues with improved selectivity. Unfortunately, no general synthetic pathway to such derivatives exists. Herein we report a four-step process that transforms inexpensive benzoic acid into 22 different quaternary carbon-containing phenanthridinone analogues with a variety of substituents on all three rings: alkyl groups at the quaternary center; methyl, methoxymethyl, or para-methoxybenzyl on the amide nitrogen; and halogen and methyl substituents on the aryl ring. Good to very good enantioselectivity was demonstrated in the key intramolecular desymmetrizing Mizoroki–Heck reaction. Transformations of the Heck reaction products into molecules with potentially greater therapeutic relevance were also accomplished.

Stereocontrolled total synthesis of (-)-myriocin

Inai, Makoto,Goto, Toshihiro,Furuta, Takumi,Wakimoto, Toshiyuki,Kan, Toshiyuki

scheme or table, p. 2771 - 2773 (2009/06/18)

The stereocontrolled total synthesis of (-)-myriocin 1 is reported. Optically active epoxide 9 was converted from symmetrical cyclohexadiene 8, utilizing an enzymatic kinetic resolution. The three sequential stereogenic centers of 1 were constructed by a regioselective epoxide-opening reaction and a Hofmann rearrangement. Elongation of the side chain was efficiently accomplished by the Julia-Kocienski reaction.

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