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66774-80-9

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66774-80-9 Usage

Uses

Vitamin D analog.

Check Digit Verification of cas no

The CAS Registry Mumber 66774-80-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,7,7 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 66774-80:
(7*6)+(6*6)+(5*7)+(4*7)+(3*4)+(2*8)+(1*0)=169
169 % 10 = 9
So 66774-80-9 is a valid CAS Registry Number.
InChI:InChI=1/C20H30O4S/c1-14-6-8-16(9-7-14)25(22,23)24-13-15(2)17-10-11-18-19(21)5-4-12-20(17,18)3/h6-9,15,17-19,21H,4-5,10-13H2,1-3H3/t15-,17-,18+,19?,20?/m1/s1

66774-80-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Inhoffen Lythgoe Diol Monotosylate

1.2 Other means of identification

Product number -
Other names (S)-2-[(1R,3aR,4S,7aR)-octahydro-4-hydroxy-7a-methyl-1H-inden-1-yl]propyl 4-methylbenzenesulfonate

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:66774-80-9 SDS

66774-80-9Downstream Products

66774-80-9Relevant articles and documents

Synthesis and biological evaluation of calcioic acid

Arnold, Leggy A.,Di Milo, Elliot S.,Mutchie, Tania R.,Yu, Olivia B.

, (2019/11/25)

Herein, we describe the synthesis of calcioic acid following a recently developed synthetic strategy for calcitroic acid. Several improvements to reaction conditions were made, which resulted in higher yields. The improved workup and isolation procedures

A protecting group-free synthesis of (-)-hortonones A-C from the Inhoffen-Lythgoe diol

Stambulyan, Hovsep,Minehan, Thomas G.

supporting information, p. 8728 - 8731 (2016/10/03)

A synthesis of hortonones A-C has been accomplished from vitamin D2via the Inhoffen-Lythgoe diol without the use of protective groups. Key steps in the syntheses include a TMS-diazomethane mediated regioselective homologation of the cyclohexano

Synthesis and preliminary biological evaluation of new antiproliferative aromatic analogues of 1α,25-dihydroxyvitamin D3

Thomas, Emmanuel,Brion, Jean-Daniel,Peyrat, Jean-Fran?ois

, p. 381 - 393 (2014/11/07)

In an effort to develop novel vitamin D3 analogues, a series of aromatic compounds was synthetized, using efficient Negishi cross coupling between alkenylzinc reagents of the C,D-ring moiety of vitamin D3, and various substituted aromatic halides as A-ring mimics. The study aimed at exploring the influence of the replacement of the original vitamin D3 diene by a styrene unit on the biological activities. Potency in the induction of the differentiation of HL-60 cells for the lead compound 36 was 12 fold less important than calcitriol correlating with a weaker binding affinity for VDR.

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