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16618-67-0

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16618-67-0 Usage

Chemical Properties

brown solid

Check Digit Verification of cas no

The CAS Registry Mumber 16618-67-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,1 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 16618-67:
(7*1)+(6*6)+(5*6)+(4*1)+(3*8)+(2*6)+(1*7)=120
120 % 10 = 0
So 16618-67-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H6BrNO3/c1-12-7-3-5(8)2-6(4-7)9(10)11/h2-4H,1H3

16618-67-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Bromo-3-Methoxy-5-Nitrobenzene

1.2 Other means of identification

Product number -
Other names 1-Bromo-3-methoxy-5-nitrobenzene

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:16618-67-0 SDS

16618-67-0Relevant articles and documents

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Elion,Janssen

, p. 194 (1925)

-

Synthesis of 1,5-bifunctional organolithium reagents by a double directed ortho-metalation: Direct transformation of esters into 1,8-dimethoxy-acridinium salts

Fischer, Christian,Sparr, Christof

, p. 5486 - 5493 (2018/05/29)

The impact of electronic and steric factors on the selectivity of the electrophilic aromatic substitution amounts to several limitations in accessing specific substitution patterns. Nucleophiles generated by directed metalation represent an effective alte

PROTEIN KINASE INHIBITORS

-

Paragraph 0787, (2015/02/18)

A compound of formula (I), wherein R3, R4, G, B, M, and Z are as defined in the claims, and pharmaceutically acceptable salts thereof are disclosed. The compounds of formula (I) possess utility as FGFR inhibitors and are useful in the treatment of a condition, where FGFR kinase inhibition is desired, such as cancer.

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