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777859-74-2

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777859-74-2 Usage

General Description

Benzoic acid, 2-bromo-6-(bromomethyl)-, methyl ester is a chemical compound with the molecular formula C9H8Br2O2. It is a methyl ester derivative of benzoic acid and contains two bromine atoms. Benzoic acid, 2-broMo-6-(broMoMethyl)-, Methyl ester is used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is also used as a building block for the synthesis of various organic compounds in the chemical industry. Benzoic acid, 2-bromo-6-(bromomethyl)-, methyl ester is a colorless to pale yellow liquid with a pungent odor and is flammable. It is important to handle this compound with caution and follow proper safety protocols when working with it in a laboratory or industrial setting.

Check Digit Verification of cas no

The CAS Registry Mumber 777859-74-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,7,8,5 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 777859-74:
(8*7)+(7*7)+(6*7)+(5*8)+(4*5)+(3*9)+(2*7)+(1*4)=252
252 % 10 = 2
So 777859-74-2 is a valid CAS Registry Number.

777859-74-2SDS

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 2-bromo-6-(bromomethyl)benzoate

1.2 Other means of identification

Product number -
Other names -

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:777859-74-2 SDS

777859-74-2Relevant articles and documents

ISOINDOLINES AS HDAC INHIBITORS

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Paragraph 00124, (2019/11/12)

The present disclosure relates to inhibitors of zinc-dependent histone deacetylases (HDACs), having the formula: (I) wherein Z, X1, X2, Y1, Y2, Y3, L, Z, and R are described herein.

NOVEL INHIBITOR COMPOUNDS OF PHOSPHODIESTERASE TYPE 10A

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, (2013/02/28)

The present invention relates to novel carboxamide compounds, pharmaceutical compositions containing them, and their use in therapy. The compounds possess valuable therapeutic properties and are particularly suitable for treating or controlling medical disorders selected from neurological disorders and psychiatric disorders, for ameliorating the symptoms associated with such disorders and for reducing the risk of such disorders

Substituted heterocyclic compounds and methods of use

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Page/Page column 15, (2010/02/10)

The present invention relates to compounds having the general formula or a pharmaceutically acceptable salt thereof, wherein R1 is a saturated or unsaturated 5-, 6- or 7-membered, ring containing 0, 1, 2 or 3 atoms selected from N, 0 and S, wherein the ring may be fused with a benzo group, and is substituted by 0, 1 or 2 oxo groups, and wherein R1 is additionally substituted; and R2 is a substituted C1-6alkyl. Also included is a method of prophylaxis or treatment of inflammation, rheumatoid arthritis, Pagets disease, osteoporosis, multiple myeloma, uveititis, acute or chronic myelogenous leukemia, pancreatic β cell destruction, osteoarthritis, rheumatoid spondylitis, gouty arthritis, inflammatory bowel disease, adult respiratory distress syndrome (ARDS), psoriasis, Crohn's disease, allergic rhinitis, ulcerative colitis, anaphylaxis, contact dermatitis, asthma, muscle degeneration, cachexia, Reiter's syndrome, type I diabetes, type II diabetes, bone resorption diseases, graft vs. host reaction, Alzheimer's disease, stroke, myocardial infarction, ischemia reperfusion injury, atherosclerosis, brain trauma, multiple sclerosis, cerebral malaria, sepsis, septic shock, toxic shock syndrome, fever, myalgias due to HIV-1, HIV-2, HIV-3, cytomegalovirus (CMV), influenza, adenovirus, the herpes viruses or herpes zoster infection in a mammal comprising administering an effective amount a compound as described above.

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