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62469-61-8

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62469-61-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62469-61-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,6 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62469-61:
(7*6)+(6*2)+(5*4)+(4*6)+(3*9)+(2*6)+(1*1)=138
138 % 10 = 8
So 62469-61-8 is a valid CAS Registry Number.

62469-61-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chlorobenzo[b][1,4]benzoxazepine

1.2 Other means of identification

Product number -
Other names 11-Chlordibenzo<b,f>-1,4-oxazepin

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:62469-61-8 SDS

62469-61-8Relevant articles and documents

An Alternative Approach to the Hydrated Imidazoline Ring Expansion (HIRE) of Diarene-Fused [1.4]Oxazepines

Grintsevich, Sergey,Sapegin, Alexander,Reutskaya, Elena,Peintner, Stefan,Erdélyi, Máté,Krasavin, Mikhail

, p. 5664 - 5676 (2020/07/21)

A four-step approach to the “hydrated imidazoline ring expansion” (HIRE) is presented. In most cases, the ring expansion was the sole process. However, for the first time, an alternative course of the hydrated imidazoline evolution was discovered which gave N-aminoethyl derivatives. These can, in principle, be converted into the target HIRE products under sufficiently forcing conditions. The approach offers improved flexibility with respect to the peripheral substituents and is also applicable to the synthesis of eleven-membered lactams. We observed that the latter can exist in two stable isomeric forms due to lactam–amide bond isomerization. The latter finding further demonstrates the value of medium-sized rings as multiple-conformer probes for biological target interrogation.

Methods for Treating Cognitive Disorders Using Inhibitors of Histone Deacetylase

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Paragraph 0399, (2017/01/23)

This disclosure relates to compounds for the inhibition of histone deacetylase and treatment of a cognitive disorder or deficit. More particularly, the disclosure provides for compounds of formula (I) wherein Q, J, L and Z are as defined in the specification.

INHIBITORS OF HISTONE DEACETYLASE

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Page/Page column 60, (2010/01/29)

Compounds which are histone deacetylase inhibitors and their use in treating various disorders, including Alzheimer's Disease.

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