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(7S)-3',4',6,8-Tetrahydro-6',7'-dimethoxy-2'-methyl-6-methylenespiro[7H-indeno[4,5-d]-1,3-dioxole-7,1'(2'H)-isoquinoline] is an alkaloid derived from Corydalis ochotensis, which is an amorphous yellow-brown substance. It forms a crystalline methiodide with a melting point of 225°C (dec.) and exhibits optical rotation of [α]D + 49.2° (c 0.2, MeOH). The ultraviolet spectrum of the free base in MeOH has two absorption maxima at 226 and 287 mJi. Upon hydrogenation over Pd-C, it yields a non-crystalline dihydro derivative with [α]D + 112°, while the dihydromethine is crystalline, with a melting point of 92°C.

4829-36-1

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4829-36-1 Usage

Uses

1. Used in Pharmaceutical Industry:
(7S)-3',4',6,8-Tetrahydro-6',7'-dimethoxy-2'-methyl-6-methylenespiro[7H-indeno[4,5-d]-1,3-dioxole-7,1'(2'H)-isoquinoline] is used as a pharmaceutical compound for its potential therapeutic applications. The alkaloid's unique chemical structure and properties make it a promising candidate for the development of new drugs targeting various health conditions.
2. Used in Chemical Research:
In the field of chemical research, (7S)-3',4',6,8-Tetrahydro-6',7'-dimethoxy-2'-methyl-6-methylenespiro[7H-indeno[4,5-d]-1,3-dioxole-7,1'(2'H)-isoquinoline] serves as a valuable compound for studying its chemical properties, reactivity, and potential applications in the synthesis of other complex molecules.
3. Used in Analytical Chemistry:
The alkaloid can be employed in analytical chemistry for the development of new methods and techniques for the identification, quantification, and analysis of similar compounds. Its unique optical rotation and ultraviolet spectrum properties can be utilized for the establishment of new analytical protocols.
4. Used in Material Science:
The crystalline nature of the dihydromethine derivative of (7S)-3',4',6,8-Tetrahydro-6',7'-dimethoxy-2'-methyl-6-methylenespiro[7H-indeno[4,5-d]-1,3-dioxole-7,1'(2'H)-isoquinoline] makes it a potential candidate for material science applications, where its structural properties can be explored for the development of new materials with specific characteristics.

References

Manske., Can. J. Res., 16B, 81 (1938)Manske., ibid, 18B, 75 (1940)McLean, Mei-Sie Lin., Tetrahedron Lett., 3819 (1964)Synthesis: McLean, Mei-Sie Lin, Whelan., Tetrahedron Lett., 2425 (1968)Irie, Kishimoto, Uyeo., J. Chern. Soc., C, 3051 (1968)

Check Digit Verification of cas no

The CAS Registry Mumber 4829-36-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,2 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4829-36:
(6*4)+(5*8)+(4*2)+(3*9)+(2*3)+(1*6)=111
111 % 10 = 1
So 4829-36-1 is a valid CAS Registry Number.

4829-36-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-6',7'-dimethoxy-2'-methyl-6-methylene-6,8,3',4'-tetrahydro-2'H-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinoline]

1.2 Other means of identification

Product number -
Other names Ochotensimin

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:4829-36-1 SDS

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