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78471-43-9

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78471-43-9 Usage

Uses

Methyl 4-bromo-2-(bromomethyl)benzoate is used as pharmaceutical intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 78471-43-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,4,7 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 78471-43:
(7*7)+(6*8)+(5*4)+(4*7)+(3*1)+(2*4)+(1*3)=159
159 % 10 = 9
So 78471-43-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H8Br2O2/c1-13-9(12)8-3-2-7(11)4-6(8)5-10/h2-4H,5H2,1H3

78471-43-9 Well-known Company Product Price

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  • Alfa Aesar

  • (H52350)  Methyl 4-bromo-2-(bromomethyl)benzoate, 96%   

  • 78471-43-9

  • 250mg

  • 980.0CNY

  • Detail
  • Alfa Aesar

  • (H52350)  Methyl 4-bromo-2-(bromomethyl)benzoate, 96%   

  • 78471-43-9

  • 1g

  • 2940.0CNY

  • Detail

78471-43-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 4-bromo-2-bromomethylbenzoate

1.2 Other means of identification

Product number -
Other names methyl 4-bromo-2-(bromomethyl)benzoate

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:78471-43-9 SDS

78471-43-9Relevant articles and documents

Discovery and biological profile of isoindolinone derivatives as novel metabotropic glutamate receptor 1 antagonists: A potential treatment for psychotic disorders

Ito, Satoru,Hirata, Yukari,Nagatomi, Yasushi,Satoh, Atsushi,Suzuki, Gentaroh,Kimura, Toshifumi,Satow, Akio,Maehara, Shunsuke,Hikichi, Hirohiko,Hata, Mikiko,Ohta, Hisashi,Kawamoto, Hiroshi

, p. 5310 - 5313 (2009)

We describe here the discovery and biological profile of a series of isoindolinone derivatives as developed mGluR1 antagonists. Our combined strategy of rapid parallel synthesis and conventional medicinal optimization successfully led to N-cyclopropyl 22 and N-isopropyl isoindolinone analogs 21 and 23 with improved in vivo DMPK profiles. Moreover the most advanced analog 23 showed an oral antipsychotic-like effect at a dose of 1 mg/kg in an animal model.

CC-90009: A Cereblon E3 Ligase Modulating Drug That Promotes Selective Degradation of GSPT1 for the Treatment of Acute Myeloid Leukemia

Hansen, Joshua D.,Correa, Matthew,Alexander, Matt,Nagy, Mark,Huang, Dehua,Sapienza, John,Lu, Gang,Lebrun, Laurie A.,Cathers, Brian E.,Zhang, Weihong,Tang, Yang,Ammirante, Massimo,Narla, Rama K.,Piccotti, Joseph R.,Pourdehnad, Michael,Lopez-Girona, Antonia

, p. 1835 - 1843 (2021/03/09)

Acute myeloid leukemia (AML) is marked by significant unmet clinical need due to both poor survival and high relapse rates where long-term disease control for most patients with relapsed or refractory AML remain dismal. Inspired to bring novel therapeutic options to these patients, we envisioned protein degradation as a potential therapeutic approach for the treatment of AML. Following this course, we discovered and pioneered a novel mechanism of action which culminated in the discovery of CC-90009. CC-90009 represents a novel protein degrader and the first cereblon E3 ligase modulating drug to enter clinical development that specifically targets GSPT1 (G1 to S phase transition 1) for proteasomal degradation. This manuscript briefly summarizes the mechanism of action, scientific rationale, medicinal chemistry, pharmacokinetic properties, and efficacy data for CC-90009, which is currently in phase 1 clinical development.

MONO HALOGEN OR METHYL-SUBSTITUTED 5-HT2B ANTAGONISTS WITH INCREASED ACTIVITY

-

Paragraph 0048; 0062, (2020/05/13)

Disclose herein are mono halogen or methyl-substituted 5-HT 2B antagonist compounds, which have been found with increased binding activity to 5-HT 2B receptor due to the substitution of halogen or methyl, and the method of using the compounds of treating or preventing a disorder mediated by 5-HT 2B.

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