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905710-14-7

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  • SAGECHEM/tert-Butyl 5-bromo-3-(hydroxymethyl)-1H-indole-1-carboxylate/SAGECHEM/Manufacturer in China

    Cas No: 905710-14-7

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905710-14-7 Usage

General Description

1-Boc-5-bromo-3-hydroxymethylindole is a chemical compound with the molecular formula C15H17BrN2O3. It is an indole derivative that contains a tert-butoxycarbonyl (Boc) protecting group. The compound is also substituted with a bromine atom and a hydroxymethyl group at the 5 and 3 positions, respectively. It is commonly used in organic synthesis as a building block for the preparation of various pharmaceuticals and agrochemicals. The presence of the Boc protecting group allows for selective reactions and can be removed under mild conditions, making it a versatile intermediate in the synthesis of complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 905710-14-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,5,7,1 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 905710-14:
(8*9)+(7*0)+(6*5)+(5*7)+(4*1)+(3*0)+(2*1)+(1*4)=147
147 % 10 = 7
So 905710-14-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H16BrNO3/c1-14(2,3)19-13(18)16-7-9(8-17)11-6-10(15)4-5-12(11)16/h4-7,17H,8H2,1-3H3

905710-14-7SDS

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 tert-butyl 5-bromo-3-(hydroxymethyl)indole-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-Boc-5-Bromo-3-hydroxymethylindole

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:905710-14-7 SDS

905710-14-7Downstream Products

905710-14-7Relevant articles and documents

Investigation into factors influencing stereoselectivity in the reactions of heterocycles with donor-acceptor-substituted rhodium carbenoids

Hedley, Simon J.,Ventura, Dominic L.,Dominiak, Paulina M.,Nygren, Cara L.,Davies, Huw M. L.

, p. 5349 - 5356 (2006)

Rhodium-catalyzed decomposition of aryldiazoacetates in the presence of pyrroles or furans results in mono- or biscyclopropanation of the heterocycle, but with opposite enantioinduction, In the absence of sterically encumbering groups, the cyclopropanatio

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