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53685-07-7

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53685-07-7 Usage

Description

Methyl 3,4-O-Isopropylidene-6-O-trityl-α-D-galactopyranoside, with the CAS number 53685-07-7, is a complex organic compound that plays a significant role in the field of organic synthesis. It is characterized by its white foam appearance and is known for its unique chemical properties that make it a valuable component in various chemical reactions and processes.

Uses

Used in Organic Synthesis:
Methyl 3,4-O-Isopropylidene-6-O-trityl-α-D-galactopyranoside is used as a key intermediate in organic synthesis for the development of various complex organic molecules. Its unique structure allows it to participate in a wide range of chemical reactions, making it a versatile building block for creating novel compounds with potential applications in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Methyl 3,4-O-Isopropylidene-6-O-trityl-α-D-galactopyranoside is used as a starting material for the synthesis of various pharmaceutical compounds. Its unique chemical properties enable the development of new drugs with improved efficacy and reduced side effects, contributing to the advancement of medical treatments.
Used in Chemical Research:
Methyl 3,4-O-Isopropylidene-6-O-trityl-α-D-galactopyranoside is also utilized in chemical research as a model compound for studying the properties and reactivity of complex organic molecules. Its unique structure provides valuable insights into the behavior of similar compounds, aiding in the development of new synthetic strategies and methodologies.
Used in Material Science:
In the field of material science, Methyl 3,4-O-Isopropylidene-6-O-trityl-α-D-galactopyranoside is used as a component in the development of novel materials with specific properties. Its unique chemical structure can be exploited to create materials with enhanced performance characteristics, such as improved mechanical strength, thermal stability, or chemical resistance.

Check Digit Verification of cas no

The CAS Registry Mumber 53685-07-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,8 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 53685-07:
(7*5)+(6*3)+(5*6)+(4*8)+(3*5)+(2*0)+(1*7)=137
137 % 10 = 7
So 53685-07-7 is a valid CAS Registry Number.
InChI:InChI=1/C29H32O6/c1-28(2)34-25-23(33-27(31-3)24(30)26(25)35-28)19-32-29(20-13-7-4-8-14-20,21-15-9-5-10-16-21)22-17-11-6-12-18-22/h4-18,23-27,30H,19H2,1-3H3/t23?,24?,25-,26?,27-/m0/s1

53685-07-7SDS

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 Methyl 3,4-O-isopropylidene-6-O-triphenylmethyl-α-D-galactopyranoside

1.2 Other means of identification

Product number -
Other names METHYL 3,4-O-ISOPROPYLIDENE-6-O-TRITYL-A-D-GALACTOPYRANOSIDE

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:53685-07-7 SDS

53685-07-7Relevant articles and documents

Novel synthesis of monosulphated methyl α-D-galactopyranosides

Rashid, Abdul,Mackie, William,Colquhoun, Ian J.,Lamba, Doriano

, p. 1122 - 1127 (2007/10/02)

The syntheses of the methyl α-D-galactopyranoside 2-,3-,4-, and 6-sulphates (11, 12, 16, and 21 respectively) have been achieved using trimethylamine - sulphur trioxide as a sulphating agent.The procedure used is high yielding and requires shorter reactio

1H- and 13C-n.m.r. spectroscopy of synthetic monosulphated methyl α-D-galactopyranosides

Contreras, Raphael Ruiz,Kamerling, Johannis P.,Breg, Jan,Vliegenthart, Johannes F. G.

, p. 411 - 418 (2007/10/02)

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Saponin and sapogenol. X. Structures of jegosapogenin and desacyljegosaponin obtained from pericarps of Styrax japonica Sieb. et Zucc.

Kitagawa,Imakura,Hayashi,Yosioka

, p. 1520 - 1531 (2007/10/07)

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