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186641-79-2

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186641-79-2 Usage

General Description

(3R)-3-Methyl-4-(tert-buty)diphenylsilyloxy)butanal is a compound that falls under the category of organosilicon compounds. It is a derivative of butanal, containing a silanol group that is protected by the tert-butyldiphenylsilyl group. (3R)-3-Methyl-4-(tert-buty)diphenylsilyloxy)butanal is often used in organic synthesis as a building block for more complex molecules. Its unique structure and functional groups make it a valuable reagent for the construction of organic molecules with specific properties and functions. Additionally, its tert-butyldiphenylsilyl group can be selectively removed under mild conditions, making it a versatile tool in synthetic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 186641-79-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,6,6,4 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 186641-79:
(8*1)+(7*8)+(6*6)+(5*6)+(4*4)+(3*1)+(2*7)+(1*9)=172
172 % 10 = 2
So 186641-79-2 is a valid CAS Registry Number.

186641-79-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (3R)-3-Methyl-4-{[(2-methyl-2-propanyl)(diphenyl)silyl]oxy}butana l

1.2 Other means of identification

Product number -
Other names (3R)-4-(tert-butyldiphenylsilyloxy)-3-methylbutanal

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:186641-79-2 SDS

186641-79-2Relevant articles and documents

Formal total synthesis of mandelalide A

Yamini,Reddy, K Mahender,Krishna, A Shiva,Lakshmi,Ghosh, Subhash

, (2019/03/23)

Abstract: In this article the formal total synthesis of mandelalide A has been described in details. The highly convergent and flexible strategy developed for mandelalide A involved the construction of key building blocks ent-9 and 7, and their assembly t

Synthesis of proposed aglycone of mandelalide A

Reddy, Karla Mahender,Yamini, Vanipenta,Singarapu, Kiran K.,Ghosh, Subhash

supporting information, p. 2658 - 2660 (2014/06/09)

A highly convergent synthesis of the proposed mandelalide A aglycone is reported. The cornerstones of the synthetic strategy include the following: E-selective intramolecular Heck cyclization, Masamune-Roush olefination, Stork-Zhao-Wittig olefination, mod

Synthesis of stereopure acyclic 1,5-dimethylalkane chirons: Building blocks of highly methyl-branched natural products

Li, Nan-Sheng,Piccirilli, Joseph A.

, p. 9633 - 9641 (2013/10/22)

An efficient synthetic method towards stereopure acyclic 1,5-dimethylalkane building blocks from methyl (2R)-3-hydroxy-2-methylpropionate (R)-1 (>99% ee) and methyl (2S)-3-hydroxy-2-methylpropionate (S)-1 (>99% ee) through a series of chemical transformat

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