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Anthracene, 9-(1-methoxyethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88474-01-5

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88474-01-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88474-01-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,4,7 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 88474-01:
(7*8)+(6*8)+(5*4)+(4*7)+(3*4)+(2*0)+(1*1)=165
165 % 10 = 5
So 88474-01-5 is a valid CAS Registry Number.

88474-01-5SDS

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 9-(1-methoxyethyl)anthracene

1.2 Other means of identification

Product number -
Other names SJGPOUFALJZJIS-UHFFFAOYSA

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:88474-01-5 SDS

88474-01-5Upstream product

88474-01-5Downstream Products

88474-01-5Relevant academic research and scientific papers

Enantioselective syntheses of candenatenins B and C using a chiral anthracene auxiliary

Jones, Amanda L.,Liu, Xiang,Snyder, John K.

scheme or table, p. 1091 - 1094 (2010/04/05)

The asymmetric syntheses of two anticancer natural products, candenatenins B and C, are described, leading to a revision of the originally assigned stereochemistries. The syntheses follow a Diels-Alder/retro-Diels Alder strategy using a chiral anthracene auxiliary to access both targets with 90% ee. The inherent structural qualities of the auxiliary allow for both regio- and diastereoselective transformations.

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