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78686-77-8

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78686-77-8 Usage

Uses

Methyl 5-Bromo-6-chloronicotinate can be used to treat diseases related to S1PR1.

Check Digit Verification of cas no

The CAS Registry Mumber 78686-77-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,6,8 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 78686-77:
(7*7)+(6*8)+(5*6)+(4*8)+(3*6)+(2*7)+(1*7)=198
198 % 10 = 8
So 78686-77-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H5BrClNO2/c1-12-7(11)4-2-5(8)6(9)10-3-4/h2-3H,1H3

78686-77-8 Well-known Company Product Price

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  • Alfa Aesar

  • (H64754)  Methyl 5-bromo-6-chloronicotinate, 98%   

  • 78686-77-8

  • 1g

  • 196.0CNY

  • Detail
  • Alfa Aesar

  • (H64754)  Methyl 5-bromo-6-chloronicotinate, 98%   

  • 78686-77-8

  • 5g

  • 706.0CNY

  • Detail
  • Alfa Aesar

  • (H64754)  Methyl 5-bromo-6-chloronicotinate, 98%   

  • 78686-77-8

  • 25g

  • 2822.0CNY

  • Detail

78686-77-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 5-bromo-6-chloronicotinate

1.2 Other means of identification

Product number -
Other names methyl 5-bromo-6-chloropyridine-3-carboxylate

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:78686-77-8 SDS

78686-77-8Relevant articles and documents

Iron-Catalyzed Amination of Strong Aliphatic C(sp3)-H Bonds

Das, Sandip Kumar,Roy, Satyajit,Khatua, Hillol,Chattopadhyay, Buddhadeb

, p. 16211 - 16217 (2020/10/26)

A concept for intramolecular denitrogenative C(sp3)-H amination of 1,2,3,4-tetrazoles bearing unactivated primary, secondary, and tertiary C-H bonds is discovered. This catalytic amination follows an unprecedented metalloradical activation mechanism. The utility of the method is showcased with the short synthesis of a bioactive molecule. Moreover, an initial effort has been embarked on for the enantioselective C(sp3)-H amination through the catalyst design. Collectively, this study underlines the development of C(sp3)-H bond functionalization chemistry that should find wide application in the context of drug discovery and natural product synthesis.

BICYCLIC HYDROXAMIC ACIDS USEFUL AS INHIBITORS OF MAMMALIAN HISTONE DEACETYLASE ACTIVITY

-

Page/Page column 107, (2017/07/14)

A compound of formula (Ia) or (Ib) or a pharmaceutically acceptable salt thereof. The compound is an inhibitor of a histone deacetylase, and as such is useful in terepy, e.g. in the treatment of autoimmune disorders, mental disorders, neurodegenerative disorders, and hyperproliferative disorders.

Design, Synthesis, and Evaluation of Novel Auxin Mimic Herbicides

Do-Thanh, Chi-Linh,Vargas, Jose J.,Thomas, Joseph W.,Armel, Gregory R.,Best, Michael D.

, p. 3533 - 3537 (2016/06/01)

Due to the key roles of auxins as master regulators of plant growth, there is considerable interest in the development of compounds with auxin-like properties for growth management and weed control applications. Herein, we describe the design and multiste

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