Welcome to LookChem.com Sign In|Join Free
  • or
Nirtetralin, derived from the Phyllanthus urinaria L. species, is a bioactive compound with significant therapeutic potential. It possesses anti-HBV (Hepatitis B Virus) activity and hepatoprotective effects, making it a valuable candidate for pharmaceutical applications.

50656-78-5

Post Buying Request

50656-78-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

50656-78-5 Usage

Uses

Used in Pharmaceutical Industry:
Nirtetralin is used as an anti-HBV agent for its ability to inhibit the replication and spread of the Hepatitis B Virus, providing a potential treatment option for individuals suffering from this viral infection.
Additionally, Nirtetralin is used as a hepatoprotective agent for its capacity to protect and repair liver cells, offering support to individuals with liver damage or dysfunction.

Check Digit Verification of cas no

The CAS Registry Mumber 50656-78-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,5 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 50656-78:
(7*5)+(6*0)+(5*6)+(4*5)+(3*6)+(2*7)+(1*8)=125
125 % 10 = 5
So 50656-78-5 is a valid CAS Registry Number.
InChI:InChI=1/C24H30O7/c1-25-11-16-8-15-10-20-23(31-13-30-20)24(29-5)22(15)21(17(16)12-26-2)14-6-7-18(27-3)19(9-14)28-4/h6-7,9-10,16-17,21H,8,11-13H2,1-5H3/t16-,17-,21+/m1/s1

50656-78-5SDS

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 5-(3,4-dimethoxyphenyl)-4-methoxy-6,7-bis(methoxymethyl)-5,6,7,8-tetrahydrobenzo[f][1,3]benzodioxole

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:50656-78-5 SDS

50656-78-5Downstream Products

50656-78-5Relevant academic research and scientific papers

Structure and Synthesis of the Aryltetralin Lignans Hypophyllanthin and Nirtetralin

Schneiders, Gail E.,Stevenson, Robert

, p. 999 - 1004 (2007/10/02)

Structures previously suggested for hypophyllanthin, the major aryltetralin lignan constituent of Phyllanthus niruri are shown to be incorrect.The structure r-1-(3,4-dimethoxyphenyl)-6-methoxy-t-2,c-3-bismethoxymethyl-7,8-methylenedioxy-1,2,3,4-tetrahydronaphthalene (5) now proposed is confirmed by an unambiguous synthesis.Synthesis of the congener, nirtetralin, is also described.

STRUCTURE AND SYNTHESYS OF HYPOPHYLLANTHIN, NIRTETRALIN, PHYLTETRALIN AND LINTETRALIN

Ganeshpure, Pralhad A.,Schneiders, Gail E,Stevenson, Robert

, p. 393 - 396 (2007/10/02)

Structures propounded for the four aryltetralin lignan constituents isolated from Phyllanthus niruri Linn. are confirmed by syntheses of their (+/-)-forms.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 50656-78-5