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155836-29-6

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155836-29-6 Usage

General Description

5-O-Methylhierochin D is a naturally occurring chemical compound found in certain plant species. It belongs to the class of alkaloids and is known for its potential pharmacological properties. 5-O-Methylhierochin D has been studied for its anti-inflammatory and antimicrobial activities, making it of interest for potential applications in medicine. Research has also suggested that 5-O-Methylhierochin D may have neuroprotective properties, and further investigation into its potential therapeutic uses is ongoing. Additionally, this compound has been identified as a potential biomarker for certain plant species, which could have implications for botanical and ecological studies.

Check Digit Verification of cas no

The CAS Registry Mumber 155836-29-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,8,3 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 155836-29:
(8*1)+(7*5)+(6*5)+(5*8)+(4*3)+(3*6)+(2*2)+(1*9)=156
156 % 10 = 6
So 155836-29-6 is a valid CAS Registry Number.

155836-29-6SDS

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 5-O-Methylhierochin D

1.2 Other means of identification

Product number -
Other names -

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:155836-29-6 SDS

155836-29-6Upstream product

155836-29-6Downstream Products

155836-29-6Relevant articles and documents

The constituents of Cistanche tubulosa (SCHRENK) HOOK. f. II. Isolation and structures of a new phenylethanoid glycoside and a new neolignan glycoside

Yoshizawa,Deyama,Takizawa,Usmanghani,Ahmad

, p. 1927 - 1930 (1990)

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Structure of barlericin, the neolignan diglycoside from Barleria acanthoides

Karim, Aman,Noor, Atia Tun,Malik, Abdul

, p. 714 - 718 (2010)

Barlericin, the new neolignan diglycoside, has been isolated from the n-butanol soluble sub-fraction of Barleria acanthoides along with dehydrodiconiferyl alcohol 12-O-β-d-glucopyranoside (2), reported for the first time from the genus Barleria. Their str

On the absolute structure of optically active neolignans containing a dihydrobenzo[b]furan skeleton

Yuen, Mabel S. M.,Xue, Feng,Mak, Thomas C. W.,Wong, Henry N. C.

, p. 12429 - 12444 (2007/10/03)

Several optically pure neolignans containing a dihydrobenzo[b]furan skeleton were synthesized. Based on an X-ray crystallographic study and circular dichroism results, the absolute configurations of some naturally occurring neolignans, namely balanophonin (1), PGI2 inducer (2), dehydrodiconiferyl alcohol-4-β-D-glucoside (3), dehydroconiferyl alcohol (4) and 3',4-di-O-methylcedrusin (5) have been unambiguously established.

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