119879-90-2 Usage
Uses
Used in Chemical Synthesis:
5-Benzyloxy-2-bromoaniline is used as a chemical intermediate for the synthesis of more complex organic compounds. Its reactive bromine atom and aniline group make it a key component in the production of various chemical products.
Used in Scientific Research:
5-Benzyloxy-2-bromoaniline is used as a research compound in the field of organic chemistry. It aids in the investigation of chemical reactions and the development of new synthetic pathways.
Used in Industrial Applications:
5-Benzyloxy-2-bromoaniline is used in various industrial processes, where its unique chemical properties contribute to the production of specialized materials and products.
Safety Precautions:
Due to its potential for causing health hazards, including skin and eye irritation, and being harmful if swallowed, 5-Benzyloxy-2-bromoaniline should be handled with care. Proper safety measures, such as wearing protective clothing and using appropriate handling equipment, should be strictly adopted while using this chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 119879-90-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,8,7 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 119879-90:
(8*1)+(7*1)+(6*9)+(5*8)+(4*7)+(3*9)+(2*9)+(1*0)=182
182 % 10 = 2
So 119879-90-2 is a valid CAS Registry Number.
119879-90-2Relevant academic research and scientific papers
BENZOCYCLOBUTANE DERIVATIVES USEFUL AS DUAL SGLT1/SGLT2 MODULATORS
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Page/Page column 95-98, (2018/05/27)
The present invention is directed to benzocyclobutane derivatives, pharmaceutical compositions containing them and their use in the treatment of disorders and conditions modulated by SGLT activity, more particularly dual SGLT1/2 activity. More particularly, the compounds of the present invention are useful in the treatment of for example, Type II diabetes mellitus, Syndrome X, and complications and symptoms associated with said disorders.
Synthesis of N-(phenylsulfonyl)-CI, N-((tert-butyloxy)carbonyl)-CI, CI-CDPI 1, and CI-CDPI 2: CC-1065 functional analogues incorporating the parent 1,2,7,7a-tetrahydrocycloprop[1,2-c]indol-4-one (CI) left-hand subunit
Boger, Dale L.,Wysocki Jr., Ronald J.,Ishizaki, Takayoshi
, p. 5230 - 5240 (2007/10/02)
Full details of the synthesis of N-(phenylsulfonyl)- and N-((tert-butyloxy)carbonyl)-1,2,7,7a-tetrahydrocycloprop[1,2-c]indol-4-one [N-(phenylsulfonyl)-CI (9) and N-BOC-CI (10)] constituting stable derivatives of the parent cyclopropylcyclohexadienone rin
