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279255-90-2

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279255-90-2 Usage

General Description

1H-Indole-1-carboxylic acid, 5-(hydroxymethyl)-, 1,1-dimethylethyl ester is a chemical compound with the molecular formula C17H21NO3. It is commonly known as Tert-Butyl Indole-3-Carboxylate. 1H-Indole-1-carboxylic acid, 5-(hydroxymethyl)-, 1,1-dimethylethyl ester is a t-butyl ester derivative of indole-3-carboxylic acid and is often used in the synthesis of pharmaceuticals and agrochemicals. Tert-Butyl Indole-3-Carboxylate is a white to off-white crystalline powder with a molecular weight of 287.35 g/mol. It is often employed as an intermediate in the production of various drugs and organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 279255-90-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,9,2,5 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 279255-90:
(8*2)+(7*7)+(6*9)+(5*2)+(4*5)+(3*5)+(2*9)+(1*0)=182
182 % 10 = 2
So 279255-90-2 is a valid CAS Registry Number.

279255-90-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 5-(hydroxymethyl)indole-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-Boc-5-(hydroxymethyl)-1H-Indole

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:279255-90-2 SDS

279255-90-2Relevant articles and documents

Nickel-Catalyzed Cross-Coupling of Vinyl Dioxanones to Form Enantiomerically Enriched Cyclopropanes

Guo, Yi-An,Liang, Tao,Kim, Seung Wook,Xiao, Hongde,Krische, Michael J.

, p. 6847 - 6850 (2017)

Under the conditions of nickel(0) catalysis, enantiomerically enriched vinyl dioxanones engage boroxines or B2(pin)2 in stereospecific cross-coupling to form diverse tetrasubstituted cyclopropanes bearing all-carbon quaternary stereocenters. The collective data corroborate a mechanism involving nickel(0)-mediated benzylic oxidative addition with inversion of stereochemistry followed by reversible olefin insertion to form a (cyclopropylcarbinyl)nickel complex, which upon reductive elimination releases the cyclopropane.

Sulfonamide bicyclic compounds

-

Page/Page column 7, (2010/10/20)

The invention encompasses compounds of Formula I, including pharmaceutically acceptable salts and solvates, their pharmaceutical compositions, and their uses in inhibiting β-amyloid peptide (β-AP) production.

SUBSTITUTED PYRIDINONES

-

, (2008/06/13)

Disclosed are compounds of Formula (I) and pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R4, and R5 are defined herein. These compounds are useful for treating diseases and conditions caused or exacerbated by unregulated p38 MAP Kinase and/or TNF activity. Pharmaceutical compositions containing the compounds, methods of preparing the compounds and methods of treatment using the compounds are also disclosed.

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