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(R)-(+)-1-(4-BROMOPHENYL)ETHYL ISOCYANATE is a chemical compound characterized by its molecular formula C9H8BrNO. It is a highly reactive and potentially hazardous chemical that can easily polymerize. (R)-(+)-1-(4-BROMOPHENYL)ETHYL ISOCYANATE is known for its wide range of applications in the field of chemistry, particularly in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and materials science. Its unique properties make it a valuable component in the development of new substances.

618461-78-2

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618461-78-2 Usage

Uses

Used in Pharmaceutical Industry:
(R)-(+)-1-(4-BROMOPHENYL)ETHYL ISOCYANATE is used as a key intermediate in the synthesis of various pharmaceuticals. Its reactivity allows for the creation of new drug molecules with unique therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, (R)-(+)-1-(4-BROMOPHENYL)ETHYL ISOCYANATE serves as a crucial component in the development of new agrochemicals, such as pesticides and herbicides, that can effectively control pests and weeds while minimizing environmental impact.
Used in Materials Science:
(R)-(+)-1-(4-BROMOPHENYL)ETHYL ISOCYANATE is utilized in materials science for the synthesis of advanced materials with specific properties, such as high thermal stability, chemical resistance, or unique optical characteristics.
Used as a Reagent in Organic Synthesis:
Due to its high reactivity, (R)-(+)-1-(4-BROMOPHENYL)ETHYL ISOCYANATE is employed as a reagent in various organic synthesis processes, enabling the formation of new chemical compounds with potential applications in different industries.
Used as an Intermediate in Chemical Production:
(R)-(+)-1-(4-BROMOPHENYL)ETHYL ISOCYANATE also serves as an intermediate in the production of various other chemicals, contributing to the development of new substances with diverse applications.
Safety Precautions:
Given its reactive nature, (R)-(+)-1-(4-BROMOPHENYL)ETHYL ISOCYANATE should be handled with caution. Proper safety measures, including the use of personal protective equipment and adherence to safety protocols, are essential when working with this chemical compound to prevent accidents and ensure the safety of individuals involved in its production and use.

Check Digit Verification of cas no

The CAS Registry Mumber 618461-78-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,8,4,6 and 1 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 618461-78:
(8*6)+(7*1)+(6*8)+(5*4)+(4*6)+(3*1)+(2*7)+(1*8)=172
172 % 10 = 2
So 618461-78-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H8BrNO/c1-7(11-6-12)8-2-4-9(10)5-3-8/h2-5,7H,1H3/t7-/m1/s1

618461-78-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-(+)-1-(4-BROMOPHENYL)ETHYL ISOCYANATE

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:618461-78-2 SDS

618461-78-2Relevant academic research and scientific papers

SYNTHESIS OF INHIBITORS OF 11BETA-HYDROXYSTEROID DEHYDROGENASE TYPE 1

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Page/Page column 46, (2010/04/03)

Disclosed are syntheses of 11 beta-HSD1 inhibitors and corresponding intermediates that are promising for the treatment of a variety of disease states including diabetes, metabolic syndrome, obesity, glucose intolerance, insulin resistance, hyperglycemia, hypertension, hypertension-related cardiovascular disorders, hyperlipidemia, deleterious gluco-corticold effects on neuronal function (e.g. cognitive impairment, dementia, and/or depression), elevated intra-ocular pressure, various forms of bone disease (e.g., osteoporosis), tuberculosis, leprosy (Hansen's disease), psoriasis, and impaired wound healing (e.g., in patients that exhibit impaired glucose tolerance and/or type 2 diabetes).

GLUCAGON ANTAGONISTS/INVERSE AGONISTS

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, (2008/06/13)

A novel class of compounds, which act to antagonize the action of the glucagon hormone on the glucagon receptor. Owing to their antagonizing effect of the glucagon receptor the compounds may be suitable for the treatment and/or prevention of any diseases and disorders, wherein a glucagon antagonistic action is beneficial, such as hyperglycemia, Type 1 diabetes, Type 2 diabetes, disorders of the lipid metabolism and obesity.

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