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288402-18-6

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288402-18-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 288402-18-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,8,4,0 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 288402-18:
(8*2)+(7*8)+(6*8)+(5*4)+(4*0)+(3*2)+(2*1)+(1*8)=156
156 % 10 = 6
So 288402-18-6 is a valid CAS Registry Number.

288402-18-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-carbomethoxy-2-naphthyl trifluoromethanesulfonate

1.2 Other means of identification

Product number -
Other names Methyl 3-(trifluoroMethylsulfonyloxy)-2-naphthoate

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:288402-18-6 SDS

288402-18-6Relevant articles and documents

An Improvement of the Palladium-Catalyzed [4+2] Cycloaddition of o -(Silylmethyl)benzyl Carbonates with Alkenes

Jin, Yushu,Ishizuka, Kentaro,Kuwano, Ryoichi

, p. 2488 - 2492 (2014)

The palladium complex, which is generated in situ from Pd(η 3-C3H5)Cp and tris(4-methoxy-3,5-dimethylphenyl)phosphine, catalyzed the [4+2] cycloaddition of o-(silylmethyl)benzyl carbonates with alkenes. The reaction of the

COMPOUND, COMPOSITION, ORGANIC ELECTROLUMINESCENT ELEMENT, AND ELECTRONIC APPLIANCE

-

Paragraph 0582-0583, (2019/11/21)

A compound is represented by a formula (20) below. In the formula (20), a least one pair of a pair of X21 and X22, a pair of X22 and X23 and a pair of X23 and X24 are carbon atoms to be bon

First Total Syntheses of Tetracenomycins C and X

Sato, Shogo,Sakata, Keiichiro,Hashimoto, Yoshimitsu,Takikawa, Hiroshi,Suzuki, Keisuke

supporting information, p. 12608 - 12613 (2017/09/11)

The first total syntheses of tetracenomycins C and X were achieved, featuring 1) preparation of a hexasubstituted naphthonitrile oxide by successive benzyne cycloadditions and an oxidative ring-opening reaction; 2) a novel ortho-quinone mono-acetal as the A-ring unit; 3) construction of three contiguous stereogenic centers by an asymmetric benzoin cyclization, an isoxazole oxidation, and a stereoselective reduction.

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