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Benzoic acid, 2-(methoxymethoxy)-6-methyl-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

394223-70-2

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394223-70-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 394223-70-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,4,2,2 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 394223-70:
(8*3)+(7*9)+(6*4)+(5*2)+(4*2)+(3*3)+(2*7)+(1*0)=152
152 % 10 = 2
So 394223-70-2 is a valid CAS Registry Number.

394223-70-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(methoxymethoxy)-6-methylbenzoate

1.2 Other means of identification

Product number -
Other names ethyl 2-methoxymethoxy-6-methylbenzoic acid

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:394223-70-2 SDS

394223-70-2Downstream Products

394223-70-2Relevant academic research and scientific papers

Inhibitors of DNA polymerase β from Schoepfia californica

Chen, Jie,Zhang, Yu-Huan,Wang, Li-Kai,Sucheck, Steven J.,Snow, Angela M.,Hecht, Sidney M.

, p. 2769 - 2770 (1998)

Fractionation of a hexane extract prepared from the plant Schoepfia californica was carried out by bioassay guided fractionation, affording five inhibitors of DNA polymerase β; four of these were shown to be anacardic acid and structurally related derivatives, while the fifth was oleic acid.

Total synthesis of 6-deoxydihydrokalafungin, a key biosynthetic precursor of actinorhodin, and its epimer

Ichinose, Koji,Kainuma, Mika,Katakawa, Kazuaki,Kumamoto, Takuya,Matsuo, Yoshika,Taguchi, Takaaki,Takahashi, Azusa

, (2021/10/26)

In this article, we report the total synthesis of 6-deoxydihydrokalafungin (DDHK), a key biosynthetic intermediate of a dimeric benzoisochromanequinone antibiotic, actinorhodin (ACT), and its epimer, epi-DDHK. Tricyclic hemiacetal with 3-siloxyethyl group was subjected to Et3SiH reduction to establish the 1,3-cis stereochemistry in the benzoisochromane, and a subsequent oxidation/deprotection sequence then afforded epi-DDHK. A bicyclic acetal was subjected to AlH3 reduction to deliver the desired 1,3-trans isomer in an approximately 3:1 ratio, which was subjected to a similar sequence to that used for the 1,3-cis isomer that successfully afforded DDHK. A semisynthetic approach from (S)-DNPA, an isolable biosynthetic precursor of ACT, was also examined to afford DDHK and its epimer, which are identical to the synthetic products.

NITROGEN-CONTAINING BICYCLIC HETEROCYCLES FOR USE AS ANTIBACTERIALS

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Page/Page column 57, (2010/02/07)

Cyclohexane and cyclohexene derivatives and pharmaceutically acceptable derivatives hereof useful in methods of treatment of bacterial infections in mammals, particularly man.

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