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1314705-19-5

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1314705-19-5 Usage

Type of compound

chemical compound

Type of derivative

trifluoromethanesulfonate derivative

Common use

reagent in organic synthesis

Known for

selectively protecting alcohol functionality in the presence of other reactive functional groups

Protecting group

tert-butyldiphenylsilyl (TBDPS)

Leaving group

trifluoromethanesulfonate

Utilization

frequently used in the synthesis of complex organic molecules and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 1314705-19-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,4,7,0 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1314705-19:
(9*1)+(8*3)+(7*1)+(6*4)+(5*7)+(4*0)+(3*5)+(2*1)+(1*9)=125
125 % 10 = 5
So 1314705-19-5 is a valid CAS Registry Number.

1314705-19-5SDS

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 2-((tert-butyldiphenylsilyl)oxy)ethyl trifluoromethanesulfonate

1.2 Other means of identification

Product number -
Other names Methanesulfonic acid, 1,1,1-trifluoro-, 2-[[(1,1-dimethylethyl)diphenylsilyl]oxy]ethyl ester

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:1314705-19-5 SDS

1314705-19-5Relevant articles and documents

Optimization of the Everolimus Intermediate Preparation Process: Impurity Identification Followed by One-Pot Transformation to the Desired Product

Shestakov, Aleksandr N.,Supurgibekov, Murat B.,Shpakova, Elena A.,Sharkov, Dmitrii E.

, p. 222 - 233 (2022/01/20)

An investigation of the everolimus intermediate PG-EVR preparation process resulted in the identification of three impurities PG-D,E,F constantly formed as byproducts in large amounts. Their structures were reliably established based on two-dimensional (2

Substituted Oxopyridine Derivatives and Use Thereof in the Treatment of Cardiovascular Disorders

-

, (2016/05/02)

The invention relates to substituted oxopyridine derivatives and to processes for their preparation, and also to their use for preparing medicaments for the treatment and/or prophylaxis of diseases, in particular cardiovascular disorders, preferably thrombotic or thromboembolic disorders, and oedemas, and also ophthalmic disorders.

SUBSTITUTED OXOPYRIDINE DERIVATIVES AND USE THEREOF IN THE TREATMENT OF CARDIOVASCULAR DISORDERS

-

, (2016/10/07)

The invention relates to substituted oxopyridine derivatives and to processes for their preparation, and also to their use for preparing medicaments for the treatment and/or prophylaxis of diseases, in particular cardiovascular disorders, preferably thrombotic or thromboembolic disorders, and oedemas, and also ophthalmic disorders.

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