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(16beta)-20-ethyl-1,6,16-trimethoxy-4-(methoxymethyl)aconitane-3,8,13,14-tetrol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38146-89-3

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38146-89-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38146-89-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,1,4 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 38146-89:
(7*3)+(6*8)+(5*1)+(4*4)+(3*6)+(2*8)+(1*9)=133
133 % 10 = 3
So 38146-89-3 is a valid CAS Registry Number.

38146-89-3SDS

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 Pseudoaconine

1.2 Other means of identification

Product number -
Other names Pseudaconine

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:38146-89-3 SDS

38146-89-3Downstream Products

38146-89-3Relevant academic research and scientific papers

Novel synthesis of 12,13-seco norditerpenoid alkaloids via semipinacol rearrangement and reaction with Br2-HOAc

Wang, Feng-Peng,Chen, Qiao-Hong,Li, Bo-Gang

, p. 4705 - 4712 (2001)

Treatment of 14-methylsulfonyl pseudaconine 3 with DMF-NaOH at 150 °C for 10 h afforded the desired C-nor and 12,13-seco norditerpenoid alkaloids 16α-methoxyl ketone 7 (70%) and 16β-methoxyl ketone 8 (15%) as a pair of epimers. Reaction of 7 with Br2-HOAc at room temperature for 1.5-2 h produced the phenols 9 (40%), 10 (10%) and 13 (29%). Whereas, treatment of 8 with Br2-HOAc under same conditions as the case for 7 gave phenolic compound 9 (38%) besides the by-product α-bromoketone 14 (25%).

A DITERPENOID ALKALOID FROM ACONITUM VILMORINIANUM VAR. PATENTIPILUM

Ding, Li-Sheng,Chen, Yao-Zu,Wu, Feng-E,Li, Bo-Gang

, p. 3694 - 3696 (1990)

A new diterpenoid alkaloid, patentine, has been isolated from the roots of Aconitum vilmorinianum var. patentipilum.Its structure was determined on the basis of chemical and spectral evidence.Together with this new compound, three known diterpenoid alkaloids have been isolated and identified.

Constituents of high altitude Himalayan herbs. part XX. A C-19 diterpenoid alkaloid from Aconitum balfourii

Khetwal

, p. 1364 - 1366 (2008/09/18)

A C-19 Diterpenoid alkaloid, 14-benzoylpseudaconine 1 has been isolated from the aerial parts of Aconitum balfourii and identified by MS, 1H ,13C NMR (SFORD and DEPT) as well as by chemical analysis.

3α,13-Dihydroxyforesaconitine from the Roots of Aconitum forestii Stapf

Wei-shin, Chen,Sepulveda-Boza, Silvia,Moertter, Monika,Breitmaier, Eberhard

, p. 1297 - 1302 (2007/10/02)

3α,13-Dihydroxyforesaconitine (1) was isolated from the roots of Aconitum forestii Stapf.It was identified as the 8-O-acetyl-14-O-(4-methoxybenzoyl) derivate of 3α,8β,13,14α-tetrahydroxy-1α,6α,16β-trimethoxy-4β-(methoxymethyl)aconitane (2).Substructures of 2 obtained by hydrolysis of 1 were derived from two-dimensional carbon-proton and proton-proton shift correlations.

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