27003-05-0 Usage
Uses
Used in Pharmaceutical Industry:
Benzoic acid, 3,5-dibromo-2-chlorois used as an intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into various drug molecules.
Used in Agrochemical Industry:
Benzoic acid, 3,5-dibromo-2-chlorois used as an intermediate in the synthesis of agrochemicals, contributing to the development of effective pesticides and other agricultural products.
Used in Dye Industry:
Benzoic acid, 3,5-dibromo-2-chlorois used as an intermediate in the synthesis of dyes, enabling the creation of a wide range of colorants for various applications.
Used in Organic Chemistry:
Benzoic acid, 3,5-dibromo-2-chlorois used as a reagent in organic chemistry reactions, facilitating various chemical processes and syntheses.
Used in Food and Beverage Industry:
Benzoic acid, 3,5-dibromo-2-chlorois used as a preservative in food and beverage products, helping to extend their shelf life and maintain freshness.
Used in Industrial and Commercial Applications:
Benzoic acid, 3,5-dibromo-2-chlorois used for its antimicrobial and antifungal properties, making it useful in various industrial and commercial applications to prevent the growth of harmful microorganisms.
Check Digit Verification of cas no
The CAS Registry Mumber 27003-05-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,0,0 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 27003-05:
(7*2)+(6*7)+(5*0)+(4*0)+(3*3)+(2*0)+(1*5)=70
70 % 10 = 0
So 27003-05-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H3Br2ClO2/c8-3-1-4(7(11)12)6(10)5(9)2-3/h1-2H,(H,11,12)
27003-05-0Relevant academic research and scientific papers
RENIN INHIBITORS
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Page/Page column 32, (2011/04/13)
Renin inhibitors, which are spirocyclic piperidine amides, of structural formula (I) and pharmaceutical compositions thereof useful in the treatment of cardiovascular diseases and renal insufficiency, wherein n, for each instance in which it occurs, is independently 0, 1, or 2; R1 is hydrogen, C1-6 -alkyl or C3-6 -cycloalkyl, wherein said C1-6 -alkyl or C3-6 -cycloalkyl group can be independently substituted with 1-3 halogens; A is (i) a five- or six-membered saturated or unsaturated heterocyclic or carbocyclic monocyclic ring or (ii) a five- or six-membered saturated or unsaturated heterocyclic or carbocyclic ring which is fused to another five- or six-membered saturated or unsaturated heterocyclic or carbocyclic ring, V is a bond or -(C=O)-, -CH(OH)-, -CH2- or =CH-; U is a bond or -CH2-, or for the case when V is =CH-, U is -CH=; X is =CH-, =CF-, =C(OR3)-, or -C=O-; and Y is =CH-, =CF-, =N-, or for the case when X is -C=O-, Y is -N(R3)-.
