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178738-66-4

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178738-66-4 Usage

General Description

The chemical (2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-(prop-2-enylamino)oxane-3,4,5-triol, also known as ribose or D-ribose, is a naturally occurring sugar molecule that plays a crucial role in many biological processes. It is a component of RNA, and is also involved in the production of ATP, which is the primary energy source for cells. D-ribose is also used as a supplement for improving athletic performance and for treating certain medical conditions such as chronic fatigue syndrome and fibromyalgia. It is considered safe for consumption and is readily available in the form of supplements. D-ribose has potential therapeutic applications in cardiac and neurological disorders due to its ability to improve energy production in the cells.

Check Digit Verification of cas no

The CAS Registry Mumber 178738-66-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,7,3 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 178738-66:
(8*1)+(7*7)+(6*8)+(5*7)+(4*3)+(3*8)+(2*6)+(1*6)=194
194 % 10 = 4
So 178738-66-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H17NO5/c1-2-3-10-9-8(14)7(13)6(12)5(4-11)15-9/h2,5-14H,1,3-4H2/t5-,6-,7+,8-,9+/m1/s1

178738-66-4Downstream Products

178738-66-4Relevant articles and documents

An efficient synthesis of N-allylglycosylamides from unprotected carbohydrates

Spevak, Wayne,Dasgupta, Falguni,Hobbs, Christopher J.,Nagy, Jon O.

, p. 3417 - 3422 (1996)

Synthetic, multivalent, carbohydrato assemblies are important tools in studying the avidity of many naturally occuring lectins for their ligands. This report details a simple, high-yielding three-step procedure to convert unprotected carbohydrates into N-allylglycosides. This method compliments the reductive amination procedure but allows the reducing-end pyranose ring to remain intact. No carbohydrate protecting groups are needed, and the resulting N-allylglycosylamide can be easily linked to other molecules. Two examples of analogs of silyl Lewis(x) and sulfo Lewis(X) have been derivatized by this process.

A new class of nitrosoureas. II. Synthesis and antitumor activity of 1-(2-chloroethyl)-3,3-disubstituted-1-nitrosoureas having a glucopyranosyl, mannopyranosyl or galactopyranosyl moiety

Tsujihara,Ozeki,Morikawa,Taga,Miyazaki,Kawamori,Arai

, p. 3262 - 3273 (2007/10/02)

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