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17482-09-6

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17482-09-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17482-09-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,4,8 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17482-09:
(7*1)+(6*7)+(5*4)+(4*8)+(3*2)+(2*0)+(1*9)=116
116 % 10 = 6
So 17482-09-6 is a valid CAS Registry Number.

17482-09-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl iodomethyl ether

1.2 Other means of identification

Product number -
Other names Benzyloxymethyliodid

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:17482-09-6 SDS

17482-09-6Downstream Products

17482-09-6Relevant articles and documents

Convergent, stereoselective synthesis of the GHIJ fragment of brevetoxin A

Crimmins, Michael T.,Zuccarello, J. Lucas,Cleary, Pamela A.,Parrish, Jonathan D.

, p. 159 - 162 (2007/10/03)

(Chemical Equation Presented) A stereoselective synthesis of the GHIJ fragment of brevetoxin A utilizing a convergent assembly strategy is described. Glycolate alkylation, ring-closing metathesis, and Hosomi-Sakurai reactions were central operations in the construction of the G ring and J ring subunits, which were united through a Horner-Wadsworth-Emmons coupling. Subsequent dehydrative cyclization produced an endocyclic enol ether that was further elaborated to the tetracyclic GHIJ fragment of brevetoxin A.

A convergent coupling strategy for the formation of polycyclic ethers: Stereoselective synthesis of the BCDE fragment of brevetoxin A

Crimmins, Michael T.,McDougall, Patrick J.,Emmitte, Kyle A.

, p. 4033 - 4036 (2007/10/03)

(Chemical Equation Presented) A stereoselective synthesis of the BCDE fragment of brevetoxin A has been completed. anti-Glycolate aldol, glycolate alkylation, and ring-closing metathesis reactions were employed as key bond-forming events. A convergent ass

Totalsynthese von Mycinolid V, dem Aglycon eines Makrolid-Antibioticums der Mycinamycin-Reihe

Ditrich, Klaus,Bube, Tomas,Stuermer, Rainer,Hoffmann, Reinhard W.

, p. 1016 - 1018 (2007/10/02)

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