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214282-10-7

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214282-10-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 214282-10-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,2,8 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 214282-10:
(8*2)+(7*1)+(6*4)+(5*2)+(4*8)+(3*2)+(2*1)+(1*0)=97
97 % 10 = 7
So 214282-10-7 is a valid CAS Registry Number.

214282-10-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[[2-methyl-1-oxo-1,2-dihydrophthalazin-4-yl]methoxy]benzaldehyde

1.2 Other means of identification

Product number -
Other names 4-[[2-Methyl-1-oxo-1,2-dihydro-phthalazin-4-yl]methoxy]benzaldehyde

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:214282-10-7 SDS

214282-10-7Relevant articles and documents

Novel phthalazinone and benzoxazinone containing thiazolidinediones as antidiabetic and hypolipidemic agents

Madhavan, Gurram R,Chakrabarti, Ranjan,Kumar, Sunil K.B,Misra, Parimal,Mamidi, Rao N.V.S,Balraju,Kasiram, Katneni,Babu, Ravi K,Suresh, Juluri,Lohray, Braj B,Lohray, Vidya B,Iqbal, Javed,Rajagopalan, Ramanujam

, p. 627 - 637 (2007/10/03)

We report here the synthesis of a series of 5-[4-[2-[substituted phthalazinones-2(or 4)yl]ethoxy]phenylmethyl]thiazolidine-2,4-diones and 5-[4-[2-[2,3-benzoxazine-4-one-2-yl]ethoxy]phenylmethyl]thiazolidine-2, 4-diones and their plasma glucose and plasma triglyceride lowering activity in db/db mice. In vitro PPARγ transactivation assay was performed in HEK 293T cells. In vitro and in vivo pharmacological studies showed that the phthalazinone analogue has better activity. PHT46 (compound 5a), the best compound in this series, showed better in vitro PPARγ transactivation potential than troglitazone and pioglitazone. In insulin resistant db/db mice, PHT46 showed better plasma glucose and triglyceride lowering activity than the standard drugs. Pharmacokinetic study in Wistar rats showed good systemic exposure of PHT46. Subchronic toxicity study in Wistar rats did not show any treatment-related adverse effect.

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