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121625-72-7

121625-72-7

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121625-72-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121625-72-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,6,2 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 121625-72:
(8*1)+(7*2)+(6*1)+(5*6)+(4*2)+(3*5)+(2*7)+(1*2)=97
97 % 10 = 7
So 121625-72-7 is a valid CAS Registry Number.
InChI:InChI=1/C17H25NO3/c1-10(2)9-18-11(3)12(6-15(20)21)16-13(18)7-17(4,5)8-14(16)19/h10H,6-9H2,1-5H3,(H,20,21)

121625-72-7SDS

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 2-[2,6,6-trimethyl-1-(2-methylpropyl)-4-oxo-5,7-dihydroindol-3-yl]acetic acid

1.2 Other means of identification

Product number -
Other names C 9001-GO

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:121625-72-7 SDS

121625-72-7Downstream Products

121625-72-7Relevant articles and documents

1-Isobutyl-2,6,6-trimethyl-4-oxo-4,5,6,7-tetrahydro-3-indoleacetic acid

Deepthi,Pattabhi, Vasantha,Nagarajan

, p. 100 - 102 (1999)

The title compound (C17H25NO3) is a perhydro-indoleacetic acid which exhibits hypoglycemic activity. The cyclohexyl ring adopts a sofa conformation. The molecule contains an intramolecular O-H...O hydrogen bond.

Synthesis and oral hypoglycemic properties of two 4-oxo-4,5,6,7-tetrahydroindole-3-acetic acids

Nagarajan,Talwalker,Goud,Shah,Shenoy

, p. 548 - 550 (2007/10/02)

Condensation of β-acetyl-2-hydroxy-4,4-dimethyl-6-oxo-1- cyclohexene-1-propionic acid (3) with n-butyl and isobutylamines affords the title acids 4 and 5, respectively, which show good oral hypoglycemic activity in normal rats. Acids 4 and 5, are also active in streptozocin-induced diabetic rats. Results of extensive pharmacological and acute toxicity tests are reported.

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