761-17-1 Usage
Description
Dibromoacetaldehyde diethyl acetal is a colorless liquid chemical compound with a mild, sweet odor. It is primarily used as an intermediate in the production of pharmaceuticals and organic synthesis. DIBROMOACETALDEHYDE DIETHYL ACETAL is flammable and may be harmful if inhaled, ingested, or absorbed through the skin, requiring careful handling and proper safety precautions.
Uses
Used in Pharmaceutical Industry:
Dibromoacetaldehyde diethyl acetal is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical properties make it a valuable component in the development of new drugs and medications.
Used in Organic Synthesis:
In the field of organic synthesis, dibromoacetaldehyde diethyl acetal serves as a versatile reagent and solvent for a wide range of chemical reactions. Its ability to participate in various chemical processes makes it an essential tool for creating new organic compounds and materials.
Used in Chemical Reactions:
Dibromoacetaldehyde diethyl acetal is used as a solvent or reagent in various chemical reactions. Its properties allow it to facilitate the formation of desired products, making it a useful component in the synthesis of complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 761-17-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 761-17:
(5*7)+(4*6)+(3*1)+(2*1)+(1*7)=71
71 % 10 = 1
So 761-17-1 is a valid CAS Registry Number.
761-17-1Relevant articles and documents
Divergent Synthesis of Natural Derivatives of (+)-Saxitoxin Including 11-Saxitoxinethanoic Acid
Walker, James R.,Merit, Jeffrey E.,Thomas-Tran, Rhiannon,Tang, Doris T. Y.,Du Bois
supporting information, p. 1689 - 1693 (2019/01/09)
The bis-guanidinium toxins are a collection of natural products that display nanomolar potency against select isoforms of eukaryotic voltage-gated Na+ ion channels. We describe a synthetic strategy that enables access to four of these poisons, namely 11-saxitoxinethanoic acid, C13-acetoxy saxitoxin, decarbamoyl saxitoxin, and saxitoxin. Highlights of this work include an unusual Mislow–Evans rearrangement and a late-stage Stille ketene acetal coupling. The IC50 value of 11-saxitoxinethanoic acid was measured against rat NaV1.4, and found to be 17.0 nm, similar to those of the sulfated toxins gonyautoxin II and III.