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18483-97-1

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18483-97-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18483-97-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,8 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 18483-97:
(7*1)+(6*8)+(5*4)+(4*8)+(3*3)+(2*9)+(1*7)=141
141 % 10 = 1
So 18483-97-1 is a valid CAS Registry Number.

18483-97-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-methoxybenzyloxy)tetrahydro-2H-pyran

1.2 Other means of identification

Product number -
Other names 2-[3-Methoxy-benzyloxy]-tetrahydro-pyran

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:18483-97-1 SDS

18483-97-1Relevant articles and documents

An efficient zirconia catalyst for solvent free tetrahydropyranylation of alcohols and phenols

Reddy, Benjaram M.,Sreekanth, Pavani M.

, p. 3561 - 3564 (2002)

Alcohols and phenols are tetrahydropyranylated in the presence of sulfated zirconia catalyst in good to excellent yields under solvent free conditions.

Short communication: Catalytic tetrahydropyranylation of phenols and alcohols using vanadium(V)-substituted polyoxomolybdates

Gharib, Ali,Jahangir, Manouchehr

experimental part, p. 287 - 296 (2012/05/20)

Alcohols and phenols were tetrahydropyranylated in the presence of H 7[PMo8V4O40] in good to excellent yields in acetonitrile and under solventfree reaction conditions. A mild and convenient method for the formation and deprotection of ethers (THP ethers) is described. The formation of THP ethers from the corresponding alcohols was accomplished in the presence of acid-sensitive functional groups.

Tetrahydropyranylation of alcohols under solvent-free conditions

Hajipour, Abdol R.,Kargosha, Majid,Ruoho, Arnold E.

experimental part, p. 1084 - 1091 (2009/09/08)

A green, efficient, and large-scale method for tetrahydropyranylation of alcohols in the presence of a catalytic amount of pyridinium chloride at room temperature under solvent-free conditions is reported. Copyright Taylor & Francis Group, LLC.

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