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453-09-8

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453-09-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 453-09-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,5 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 453-09:
(5*4)+(4*5)+(3*3)+(2*0)+(1*9)=58
58 % 10 = 8
So 453-09-8 is a valid CAS Registry Number.

453-09-8SDS

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 2-fluoropropane-1,3-diol

1.2 Other means of identification

Product number -
Other names 2-Fluor-propan-1,3-diol

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:453-09-8 SDS

453-09-8Relevant articles and documents

Synthesis and evaluation of N-(4-benzylphenyl)piperazines as VGF inducers

Toba, Tetsuya,Suzuki, Ryosuke,Futamura-Takahashi, Junko,Kawamoto, Yoshito,Tamura, Shigeki,Kuroda, Mariko,Shimmyo, Yoshiari,Kadokura, Michinori,Goto, Kazumichi,Inoue, Teruyoshi,Muto, Tsuyoshi,Annoura, Hirokazu

, p. 2528 - 2532 (2018/06/06)

A series of compounds was discovered that induce the production of VGF mRNA in SH-SY5Y cells and exhibit cytoprotection under tunicamycin induced endoplasmic reticulum (ER) stress. The aminophenol ring and linker chain of the template SUN N8075 (1) was modified to yield compounds with higher efficacy and lower propensity for adverse effects.

6,7-DIHYDRO-5H-PYRAZOLO[5,1-B][1,3]OXAZINE-2-CARBOXAMIDE COMPOUNDS

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Page/Page column 57, (2017/09/09)

The present invention is directed to PDE4B inhibitors of Formula I: (I) or a pharmaceutically acceptable salt thereof, wherein the substituents R1, R2, R 3, and R 4are as defined herein. The invention is also di

INHIBITORS OF AKT ACTIVITY

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Page/Page column 61, (2008/06/13)

Invented are novel 1 H-imidazo[4,5-c]pyridin-2-yl compounds, the use of such compounds as inhibitors of protein kinase B activity and in the treatment of cancer and arthritis.

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