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116174-99-3

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116174-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116174-99-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,1,7 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 116174-99:
(8*1)+(7*1)+(6*6)+(5*1)+(4*7)+(3*4)+(2*9)+(1*9)=123
123 % 10 = 3
So 116174-99-3 is a valid CAS Registry Number.

116174-99-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Agrostophyllin

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:116174-99-3 SDS

116174-99-3Downstream Products

116174-99-3Relevant articles and documents

Agrostophyllanthrol and isoagrostophyllanthrol, two novel diastereomeric phenanthropyran derivatives from the orchid Agrostophyllum khasiyanum

Majumder,Mukhoti, Nirmalendu,Chattopadhyay, Saswati

experimental part, p. 1315 - 1325 (2010/03/31)

Agrostophyllanthrol and isoagrostophyllanthrol, two novel diaslereonicric pbenanthropyran derivatives were isolated from the orchid Agrostophyllum khasiyanum which earlier afforded eleven stilbenoids, viz. the two dimeric phenanthrene derivatives agrostonin [2,2′,7,7′-tetrahydroxy-4, 4′,6,6′-tetramethoxy-l,l′-biphenanthryl] and agrostonidin [2,2′,6,6′-tetrahydroxy-4,4′,7,7′-tetramethoxy-l, l′-biphenanthryl], eight phenanthropyran derivatives imbricatin [2,7-dihydroxy-6-methoxy-9,10-dihydro-5H-phenanthro[4,5-bcd]pyran], agrostophyllidin [7-hydroxy-2,6-dimethoxy-9,10-dihydro-5H-phenanathro[4,5-bcd] pyran], agrostophylloxidin [7-hydroxy-2,5,6-triinethoxy-5H-phenanthro[4,5-bcd] pyran], flaccidinin [2,6-dihydroxy-7-methoxy-5H-phenanthro[4,5-bcd]Jpyran-5-one] , isoflaccidinin [2,7-dihydroxy-6-methoxy-5H-phenanthro[4,5-bcd]pyran-5-one], agrostophyllin [7-hydroxy-2,6-dimethoxy-5H-phenanthro[4,5-bcd]pyran], agrostophyllone [7-hydroxy- 2,6-dimethoxy-5H-phenanthro[4,5-bcd]pyran-5-one], agrostophylloxin [2,6,7-trimethoxy-5H-phenanthro[4,5-bcd]pyran-5-one] and the bibenzyl derivative moscatalin [4,4′-dihydroxy-3,3′,5- trimethoxybibenzyl]. The structures of agrostophyllanthrol and isoagrostophyllanthrol were established as 7-hydroxy-2,6-dimethoxy-5H- phenanthro[4,5-bcd]pyran-5(equat)ol and 7-hydroxy-2,6-dimethoxy-5H-phenanthro[4, 5-bcd]pyran-5(ax)ol, respectively from various spectral and chemical evidence. Agrostophyllanthrol and isoagrostophyllanthrol, thus, represent two novel examples of otherwise conformational isomers becoming highly stable diastereomers due to unusual steric hindrance to conformational flipping.

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