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Benzaldehyde, 3-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

110130-71-7

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110130-71-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110130-71-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,1,3 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 110130-71:
(8*1)+(7*1)+(6*0)+(5*1)+(4*3)+(3*0)+(2*7)+(1*1)=47
47 % 10 = 7
So 110130-71-7 is a valid CAS Registry Number.

110130-71-7SDS

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 3-[[tert-butyl(diphenyl)silyl]oxymethyl]benzaldehyde

1.2 Other means of identification

Product number -
Other names Benzaldehyde,3-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]

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:110130-71-7 SDS

110130-71-7Relevant academic research and scientific papers

AROMATIC RING COMPOUND

-

, (2015/01/18)

Provided is an aromatic ring compound having a GPR40 agonist activity. A compound represented by the formula (I): wherein each symbol is as described in the DESCRIPTION, or a salt thereof has a GPR40 agonist activity, and is useful as an agent for the prophylaxis or treatment of diabetes and the like.

Design and synthesis of potent macrocyclic renin inhibitors

Sund, Christian,Belda, Oscar,Wiktelius, Daniel,Sahlberg, Christer,Vrang, Lotta,Sedig, Susanne,Hamelink, Elizabeth,Henderson, Ian,Agback, Tatiana,Jansson, Katarina,Borkakoti, Neera,Derbyshire, Dean,Eneroth, Anders,Samuelsson, Bertil

scheme or table, p. 358 - 362 (2011/02/27)

Two types of P1-P3-linked macrocyclic renin inhibitors containing the hydroxyethylene isostere (HE) scaffold just outside the macrocyclic ring have been synthesized. An aromatic or aliphatic substituent (P3sp) was introduced in the macrocyclic ring aiming

ASYMMETRIC DITHIOACETALS III: THE PREPARATION OF THE ENANTIOMERS OF 3-((((3-(2-(7-CHLOROQUINOLIN-2-YL)-(E)-ETHENYL)PHENYL)-3-DIMETHYLAMINO-3-OXOPROPYLTHIO)METHYL)THIO)PROPIONIC ACID (L-660,711) (MK-571), AN ANTAGONIST OF LEUKOTRIENE D4

Young, Robert N.,Gauthier, Jacques Yves,Therien, Michel,Zamboni, Robert

, p. 967 - 978 (2007/10/02)

The application of a novel method for the preparation of chiral dithioacetals to the synthesis of the enantiomers of L-660,711, an antagonist of leukotriene D4, is described.Reaction of 3-(t-butyldiphenylsilyloxymethyl)benzaldehyde or isophthal

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