Welcome to LookChem.com Sign In|Join Free
  • or
(22R,23R)-2α,3α,22,23-Tetrahydroxy-5α-ergost-24(28)-en-6-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85797-15-5

Post Buying Request

85797-15-5 Suppliers

Recommended suppliers

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

85797-15-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85797-15-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,7,9 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 85797-15:
(7*8)+(6*5)+(5*7)+(4*9)+(3*7)+(2*1)+(1*5)=185
185 % 10 = 5
So 85797-15-5 is a valid CAS Registry Number.

85797-15-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name dolichosterone

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:85797-15-5 SDS

85797-15-5Downstream Products

85797-15-5Relevant academic research and scientific papers

SYNTHESIS OF NATURALLY OCCURRING BRASSINOSTEROIDS EMPLOYING CLEAVAGE OF 23,24-EPOXIDES AS KEY REACTIONS. SYNTHESIS OF BRASSINOLIDE, CASTASTERONE, DOLICHOLIDE, DOLICHOSTERONE, HOMODOLICHOLIDE, HOMODOLICHOSTERONE, 6-DEOXOCASTASTERONE AND 6-DEOXODOLICHOSTERONE

Mori, Kenji,Sakakibara, Masayuki,Okada, Katsuhide

, p. 1767 - 1782 (2007/10/02)

Eight new plant growth-promoting steroids (brassinolide, castasterone, dolicholide, dolichosterone, homodolicholide, homodolichosterone, 6-deoxocastasterone and 6-deoxodolichosterone) were synthesized by the regio- and stereoselective ring-opening reactions of 23,24-epoxides prepared from stigmasterol.

Stereoselective Synthesis of the Plant-growth-promoting Steroids Dolicholide and Dolichosterone

Takatsuto, Suguru,Ikekawa, Nobuo

, p. 2133 - 2137 (2007/10/02)

Stereoselective syntheses of dolicholide (3), (22R,23R)-2α,3α,22,23-tetrahydroxy-B-homo-7-oxa-5α-ergost-24(28)-en-6-one, and dolichosterone (4), (22R,23R)-2α,3α,22,23-tetrahydroxy-5α-ergost-24(28)-en-6-one, were achieved from the known (22E,24S)-2α,3α-diacetoxy-5α-stigmast-22-en-6-one (5) which is readily available from stigmasterol.The key step in the construction of the (22R,23R)-vicinal diol function in the steroidal side-chain was new and used the method of chelation control.

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 85797-15-5