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(22R,23R)-2α,3α,22,23-Tetrahydroxy-28-methyl-B-homo-7-oxa-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.

86630-40-2

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86630-40-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86630-40-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,6,3 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 86630-40:
(7*8)+(6*6)+(5*6)+(4*3)+(3*0)+(2*4)+(1*0)=142
142 % 10 = 2
So 86630-40-2 is a valid CAS Registry Number.

86630-40-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name homodolicholide

1.2 Other means of identification

Product number -
Other names (1R,3aS,3bS,6aS,8S,9R,10aR,10bS,12aS)-1-((E)-(1S,2R,3R)-2,3-Dihydroxy-4-isopropyl-1-methyl-hex-4-enyl)-8,9-dihydroxy-10a,12a-dimethyl-hexadecahydro-5-oxa-benzo[3,4]cyclohepta[1,2-e]inden-6-one

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:86630-40-2 SDS

86630-40-2Downstream Products

86630-40-2Relevant 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.

Short-step Syntheses of Homodolicholide and Homodolichosterone

Sakakibara, Masayuki,Mori, Kenji

, p. 745 - 752 (2007/10/02)

Short-step syntheses of homodolicholide 1 and homodolichosterone 2 are described.An (E)-geometry of their C(24)=C(28) double bond was established.Transformation reactions of the epoxy ring were applied to the syntheses, as was done in our syntheses of brassinolide and its related compounds.

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