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91661-60-8

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91661-60-8 Usage

Description

[(2R,3R,4E,6E,9R,11R,12S,13S,14R)-12-[3,6-dideoxy-3-(dimethylamino)-beta-D-galactopyranosyl]oxy-2-ethyl-14-hydroxy-5,9,13-trimethyl-8,16-dioxo-11-(2-phenoxyethyl)oxacyclohexadeca-4,6-dien-3-yl]methyl 6-deoxy-2,3-di-O-methyl-D-allopyranoside is a complex organic compound with a long, branched structure and multiple functional groups. It features a cyclohexadeca-4,6-dien-3-yl group, a phenoxyethyl group, an amine group, a galactopyranosyl group, and an ethyl group, among others. [(2R,3R,4E,6E,9R,11R,12S,13S,14R)-12-[3,6-dideoxy-3-(dimethylamino)-beta-D-galactopyranosyl]oxy-2-ethyl-14-hydroxy-5,9,13-trimethyl-8,16-dioxo-11-(2-phenoxyethyl)oxacyclohexadeca-4,6-dien-3-yl]methyl 6-deoxy-2,3-di-O-methyl-D-allopyranoside's intricate structure and diverse functional groups make it a challenging molecule to synthesize and study.

Uses

Used in Pharmaceutical Industry:
[(2R,3R,4E,6E,9R,11R,12S,13S,14R)-12-[3,6-dideoxy-3-(dimethylamino)-beta-D-galactopyranosyl]oxy-2-ethyl-14-hydroxy-5,9,13-trimethyl-8,16-dioxo-11-(2-phenoxyethyl)oxacyclohexadeca-4,6-dien-3-yl]methyl 6-deoxy-2,3-di-O-methyl-D-allopyranoside is used as a potential therapeutic agent for various medical applications due to its complex structure and the presence of multiple functional groups that can interact with biological targets.
Used in Chemical Research:
[(2R,3R,4E,6E,9R,11R,12S,13S,14R)-12-[3,6-dideoxy-3-(dimethylamino)-beta-D-galactopyranosyl]oxy-2-ethyl-14-hydroxy-5,9,13-trimethyl-8,16-dioxo-11-(2-phenoxyethyl)oxacyclohexadeca-4,6-dien-3-yl]methyl 6-deoxy-2,3-di-O-methyl-D-allopyranoside is also utilized in chemical research as a model for studying the synthesis and reactivity of complex organic molecules. Its intricate structure and diverse functional groups provide a platform for exploring new reaction pathways and developing innovative synthetic strategies.
Used in Material Science:
[(2R,3R,4E,6E,9R,11R,12S,13S,14R)-12-[3,6-dideoxy-3-(dimethylamino)-beta-D-galactopyranosyl]oxy-2-ethyl-14-hydroxy-5,9,13-trimethyl-8,16-dioxo-11-(2-phenoxyethyl)oxacyclohexadeca-4,6-dien-3-yl]methyl 6-deoxy-2,3-di-O-methyl-D-allopyranoside's unique structural features and functional groups may also find applications in material science, where it could be used to develop novel materials with specific properties, such as improved stability, reactivity, or selectivity in various chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 91661-60-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,6,6 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 91661-60:
(7*9)+(6*1)+(5*6)+(4*6)+(3*1)+(2*6)+(1*0)=138
138 % 10 = 8
So 91661-60-8 is a valid CAS Registry Number.

91661-60-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Tylosin, 4A-O-de(2,6-dideoxy-3-C-methyl-α-L-ribo-hexopyranosyl)-20-deoxo-20-phenoxy-

1.2 Other means of identification

Product number -
Other names 20-DIHYDRO-20-O-PHENYL DESMYCOSIN

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:91661-60-8 SDS

91661-60-8Downstream Products

91661-60-8Relevant articles and documents

Synthesis and Evaluation of Tylosin-Related Macrolides Modified at the Aldehyde Function: A New Series of Orally Effective Antibiotics

Kirst, Herbert A.,Toth, John E.,Debono, Manuel,Willard, Kevin E.,Truedell, Brenda A.,et al.

, p. 1631 - 1641 (2007/10/02)

Modification of the aldehyde group in tylosin and related macrolide antibiotics dramatically enhanced the oral efficacy of the derivatives against experimental infections caused by susceptible bacteria in laboratory animals.A large number and wide variety

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