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73899-15-7

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73899-15-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73899-15-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,8,9 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 73899-15:
(7*7)+(6*3)+(5*8)+(4*9)+(3*9)+(2*1)+(1*5)=177
177 % 10 = 7
So 73899-15-7 is a valid CAS Registry Number.

73899-15-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-bromophenyl)ethoxy-tert-butyl-dimethylsilane

1.2 Other means of identification

Product number -
Other names 1-<(tert-butyldimethylsilyl)oxy>-2-(4-bromophenyl)ethane

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:73899-15-7 SDS

73899-15-7Relevant articles and documents

Synthesis of an [125I]-labelled derivative of MK-571, a tool for LTD4 receptor studies

Li,Leblanc,Zamboni,Young

, p. 537 - 544 (1994)

An [125I]-labelled derivative of MK-571 2 was synthesized from the arylstanne derivative 11 in 50% radiochemical yield. Compound 2 is a useful tool for LTD4 receptor studies. The arylstanne intermediate 11 was obtained from the coupl

Synthesis of some nitroimidazole substituted boronic acids: Precursors to technetium-99m complexes with potential for imaging hypoxic tissue

Raju,Ramalingam,Nowotnik

, p. 10233 - 10238 (1992)

A number of nitroimidazole substituted alkyl and aryl-boronic acids were synthesized as precursors to technetium-99m complexes under investigation as potential imaging agents of hypoxia. Compounds were prepared with nitro group either in the 2- or 4-posit

Nitroxide derivative of ROCK kinase inhibitor

-

Paragraph 0357-0363, (2020/06/17)

The invention provides a small molecular compound of a NO donor. The small molecular compound is characterized in that the small molecular compound is a compound shown represented by structural formula I shown in the description, or a stereoisomer, a geometrical isomer, a tautomer, a racemate, a deuterated isotope derivative, a hydrate, a solvate, a metabolite, a pharmaceutically acceptable salt or a prodrug thereof; and in the formula I, ring A is a substituted or unsubstituted heteroaromatic ring, X is selected from (CH2)n, n is selected from 0, 1, 2 and 3, R is a substituent group of terminal -O-NO2, R is selected from hydrogen, a hydroxyl group, halogen, an amino group, a cyano group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkoxy group, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted alkynyl group and a substituted or unsubstituted heteroalkyl group, and R and R are respectively and independently selected from hydrogen, a substituted or unsubstituted alkyl group, a substituted or unsubstituted naphthenic base or an amino protecting group, or R and R are connected to form a substituted or unsubstituted cyclic heteroalkyl group. The compound has a high-activity inhibition effect on ROCK kinase.

ANTIMICROBIAL COMPOUNDS AND METHODS

-

Paragraph 00360, (2020/07/31)

The invention is directed to compounds that are active as antibacterial agents. The invention compounds are active against gram-positive and gram-negative bacteria and can be used to treat infections caused by gram-positive and gram-negative bacteria. Also disclosed are processes and intermediates for making the compounds.

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