2051-05-0 Usage
Description
DIAMYL SULFITE is a chemical compound characterized as a clear, colorless liquid with a fruity odor. It is insoluble in water and is recognized for its role as a reagent in organic synthesis and as an additive in the food and beverage industry.
Uses
Used in Food and Beverage Industry:
DIAMYL SULFITE is used as an antioxidant and preservative for extending the shelf life of various products such as wines, fruit juices, and baked goods. It serves to inhibit the growth of microorganisms and prevent the oxidation of food and beverages, ensuring freshness and quality over time.
Used in Organic Synthesis:
In the realm of organic synthesis, DIAMYL SULFITE is utilized as a reagent, playing a crucial role in the production and synthesis of various organic compounds. Its chemical properties make it a valuable component in the development of new substances and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 2051-05-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,5 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2051-05:
(6*2)+(5*0)+(4*5)+(3*1)+(2*0)+(1*5)=40
40 % 10 = 0
So 2051-05-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H22O3S/c1-3-5-7-9-12-14(11)13-10-8-6-4-2/h3-10H2,1-2H3
2051-05-0Relevant articles and documents
Synthesis and anti-influenza virus activity of 7-O-alkylated derivatives related to zanamivir
Honda, Takeshi,Masuda, Takeshi,Yoshida, Shuku,Arai, Masami,Kaneko, Satoru,Yamashita, Makoto
, p. 1925 - 1928 (2007/10/03)
A series of 7-alkyl ether derivatives related to zanamivir were synthesized using direct alkylation of the C-7 alcohol of sialic acid. Alkyl ether moiety of less than 12 carbons in length showed low nanomolar inhibitory activity against influenza A virus sialidase. Furthermore, their moiety improved influenza A virus plaque reduction activity compared to zanamivir. However, removal of the 8,9-diol of the 7-O-alkyl derivatives resulted in loss of antiviral potency. This result suggests that 8,9-diol must play an important role in binding with both influenza A and B virus sialidases.
