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103634-10-2

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  • [R-(Z)]-4-Hydroxy-N,N,N-trimethyl-9-oxo-7-[(triphenylmethoxy)methyl]-3,5,8-trioxa-4-phosphahexacos-17-en-1-aminium 4-Oxide Inner Salt

    Cas No: 103634-10-2

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  • [R-(Z)]-4-Hydroxy-N,N,N-trimethyl-9-oxo-7-[(triphenylmethoxy)methyl]-3,5,8-trioxa-4-phosphahexacos-17-en-1-aminium 4-Oxide Inner Salt

    Cas No: 103634-10-2

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103634-10-2 Usage

Description

[R-(Z)]-4-Hydroxy-N,N,N-triMethyl-9-oxo-7-[(triphenylMethoxy)Methyl]-3,5,8-trioxa-4-phosphahexacos-17-en-1-aMiniuM 4-Oxide Inner Salt is a complex organic compound with a unique molecular structure. It is characterized by its pale yellow solid appearance and serves as an intermediate in the synthesis of glycerophospholipids, which are essential for regulating various enzyme activities.

Uses

Used in Pharmaceutical Industry:
[R-(Z)]-4-Hydroxy-N,N,N-triMethyl-9-oxo-7-[(triphenylMethoxy)Methyl]-3,5,8-trioxa-4-phosphahexacos-17-en-1-aMiniuM 4-Oxide Inner Salt is used as an intermediate in the synthesis of glycerophospholipids for its role in regulating enzyme activities. This makes it a valuable component in the development of pharmaceuticals targeting various diseases and conditions.
Used in Biochemical Research:
In the field of biochemical research, [R-(Z)]-4-Hydroxy-N,N,N-triMethyl-9-oxo-7-[(triphenylMethoxy)Methyl]-3,5,8-trioxa-4-phosphahexacos-17-en-1-aMiniuM 4-Oxide Inner Salt is utilized for studying the mechanisms of enzyme regulation and the role of glycerophospholipids in cellular processes. This helps researchers gain a deeper understanding of biological systems and develop new therapeutic strategies.
Used in Cosmetics Industry:
[R-(Z)]-4-Hydroxy-N,N,N-triMethyl-9-oxo-7-[(triphenylMethoxy)Methyl]-3,5,8-trioxa-4-phosphahexacos-17-en-1-aMiniuM 4-Oxide Inner Salt may also find applications in the cosmetics industry, where it can be used as an active ingredient in skincare products. Its role in enzyme regulation and its potential effects on cellular processes could contribute to the development of innovative cosmetic formulations with anti-aging, moisturizing, or other beneficial properties.

Check Digit Verification of cas no

The CAS Registry Mumber 103634-10-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,6,3 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 103634-10:
(8*1)+(7*0)+(6*3)+(5*6)+(4*3)+(3*4)+(2*1)+(1*0)=82
82 % 10 = 2
So 103634-10-2 is a valid CAS Registry Number.

103634-10-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2R)-2-[(Z)-octadec-9-enoyl]oxy-3-trityloxypropyl] 2-(trimethylazaniumyl)ethyl phosphate

1.2 Other means of identification

Product number -
Other names 1-O-trityl-2-oleoyl-sn-glycero-3-phosphocholine

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:103634-10-2 SDS

103634-10-2Relevant articles and documents

Synthesis of phosphatidylcholines containing ricinoleic acid

Borsotti, Gianpietro,Guglielmetti, Gianfranco,Spera, Silvia,Battistel, Ezio

, p. 10219 - 10227 (2001)

1,2-Diricinoleoyl- and 1-ricinoleoyl-2-oleoyl-sn-glycero-3-phosphocholine were synthesised with good yields. The synthesis started with the preparation of ricinoleic acid from castor oil. The choice of a suitable agent to protect the -OH group of ricinoleic acid was a key factor to afford the final products. Several protecting groups were assayed but only β-methoxyethoxymethyl chloride (MEMCl) and 2,2,2-trichloroethyl chloroformate (TRECCl) gave reasonable yields and good optical purities of the final products. The overall yields for 1,2-diricinoleoyl-sn-glycero-3-phosphocholine and 1-ricinoleoyl-2-oleoyl-sn-glycero-3-phosphocholine were 32.1% (with respect to ricinoleic acid methyl ester using TREC as protecting group) and 10.3% (with respect to 1-trityl-glycero-3-phosphocholine), respectively.

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