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87407-73-6

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  • 3-[7A-METHYL-1-(1,4,5-TRIMETHYL-HEX-2-ENYL)-OCTAHYDRO-INDEN-4-YLIDENEMETHYL]-2,2-DIOXO-2,3,4,5,6,7-HEXAHYDRO-1H-2L6-BENZO[C]THIOPHEN-5-OL

    Cas No: 87407-73-6

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87407-73-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87407-73-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,4,0 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 87407-73:
(7*8)+(6*7)+(5*4)+(4*0)+(3*7)+(2*7)+(1*3)=156
156 % 10 = 6
So 87407-73-6 is a valid CAS Registry Number.
InChI:InChI=1/C28H44O3S/c1-18(2)19(3)8-9-20(4)25-12-13-26-21(7-6-14-28(25,26)5)15-27-24-16-23(29)11-10-22(24)17-32(27,30)31/h8-9,15,18-20,23,25-27,29H,6-7,10-14,16-17H2,1-5H3/b9-8+,21-15-/t19-,20+,23?,25+,26?,27?,28+/m0/s1

87407-73-6SDS

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 Benzo[c]thiophene-5-ol, 1,3,4,5,6,7-hexahydro-3-[(E)-[(1R,3aS,7aR)-octahydro-7a-methyl-1-[(1R,2E,4R)-1,4,5-trimethyl-2-hexen-1-yl]-4H-inden-4-ylidene]methyl]-, 2,2-dioxide, (3S,6S)-

1.2 Other means of identification

Product number -
Other names 9,10-Secoergosta-5(10),7,22-trien-3-ol, 6,19-sulfonyl-, (3β,6S,7E,22E)-

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:87407-73-6 SDS

87407-73-6Downstream Products

87407-73-6Relevant articles and documents

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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