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4-BROMO-7-BENZYLOXY-1H-INDOLE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

476622-92-1

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476622-92-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 476622-92-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,6,6,2 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 476622-92:
(8*4)+(7*7)+(6*6)+(5*6)+(4*2)+(3*2)+(2*9)+(1*2)=181
181 % 10 = 1
So 476622-92-1 is a valid CAS Registry Number.

476622-92-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-BROMO-7-BENZYLOXY-1H-INDOLE

1.2 Other means of identification

Product number -
Other names 7-(benzyloxy)-4-bromo-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:476622-92-1 SDS

476622-92-1Downstream Products

476622-92-1Relevant academic research and scientific papers

INDOLES AS 5-HT6 MODULATORS

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Page/Page column 132, (2008/06/13)

The present invention relates to novel compounds of formula (I) wherein m, n, R0, R1, R2, R3 and R4 are as described herein, to pharmaceutical compositions comprising the compounds, to processes for t

The first total synthesis of dragmacidin D

Garg, Neil K.,Sarpong, Richmond,Stoltz, Brian M.

, p. 13179 - 13184 (2007/10/03)

The first total synthesis of the biologically significant bis-indole alkaloid dragmacidin D (5) has been achieved. Thermal and electronic modulation provides the key for a series of palladium-catalyzed Suzuki cross-coupling reactions that furnished the core structure of the complex guanidine- and aminoimidazole-containing dragmacidins. Following this crucial sequence, a succession of meticulously controlled final events was developed leading to the completion of the natural product.

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