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tert-Butyl-dimethyl-{(S)-3-[(R)-7a-methyl-1-((E)-(1R,4R)-1,4,5-trimethyl-hex-2-enyl)-octahydro-inden-(4E)-ylidenemethyl]-2,2-dioxo-2,3,4,5,6,7-hexahydro-1H-2λ6-benzo[c]thiophen-5-yloxy}-silane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87417-27-4

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87417-27-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87417-27-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,4,1 and 7 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 87417-27:
(7*8)+(6*7)+(5*4)+(4*1)+(3*7)+(2*2)+(1*7)=154
154 % 10 = 4
So 87417-27-4 is a valid CAS Registry Number.

87417-27-4Downstream Products

87417-27-4Relevant academic research and scientific papers

Synthesis of 24(28)-methylene-1α-hydroxyvitamin D3, a novel vitamin D3 analogue

Guo, Wei,Fang, Zhijie,Li, Hongliang,Liu, Yanan

, p. 231 - 235 (2014/05/06)

24(28)-Methylene-1α-hydroxyvitamin D3 was synthesised in 13 steps from vitamin D2. The key step of the synthesis involved the Wittig-Horner olefination of a nor-vitamin D2 aldehyde with diethylphosphono-3-methyl-2-butanone

Improved and efficient synthesis of Maxacalcitol

Feng, Shi,Cui, Li-Fei,Wei, He-Geng,Zheng, Guo-Jun,Wang, Ya-Ping,Wang, Xiang-Jing,Zhang, Ji,Xiang, Wen-Sheng

, p. 771 - 774 (2014/06/09)

Maxacalcitol, the 22-oxa-derivative of 1α, 25-dihydroxyvitamin D 3, has been used as an antihyperparathyroidism and antipsoriatic drug. In this paper, an alternative synthetic route has been developed using commercially available vitamin D

Development of an improved process for doxercalciferol via a continuous photochemical reaction

Anderson, Bruce G.,Bauta, William E.,Cantrell, William R.

, p. 967 - 975 (2012/08/27)

Doxercalciferol (1α-hydroxyvitamin D2) is a commercially approved vitamin D derivative used to treat chronic kidney disease (CKD) patients whose kidneys cannot metabolically introduce a hydroxyl group at C1. A new process for the production of doxercalcif

An improved synthesis of 24,24-difluoro-1α,25-dihydroxyvitamin D3 from readily available vitamin D2

Ando,Koike,Takayama

, p. 189 - 192 (2007/10/02)

An improved synthesis of a highly potent vitamin D3 analog, 24,24-difluoro-1α,25-dihydroxyvitamin D3 (1b) has been accomplished via vitamin D2-SO2 adducts. The introduction of fluorine atoms was performed by tre

An improved synthesis of 24,24-difluoro-1α,25-dihydroxy-vitamin D3 from vitamin D2

Ando,Kondo,Koike,Takayama

, p. 1662 - 1664 (2007/10/02)

An improved synthesis of a highly potent vitamin D3 analog, 24,24-difluoro-1α,25-dihydroxyvitamin D3 has been accomplished. The total yield was 9.3% from inexpensive vitamin D2 in 11 steps.

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