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174626-26-7

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174626-26-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 174626-26-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,6,2 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 174626-26:
(8*1)+(7*7)+(6*4)+(5*6)+(4*2)+(3*6)+(2*2)+(1*6)=147
147 % 10 = 7
So 174626-26-7 is a valid CAS Registry Number.

174626-26-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(phenylmethoxycarbonylamino)butyl methanesulfonate

1.2 Other means of identification

Product number -
Other names -

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:174626-26-7 SDS

174626-26-7Relevant articles and documents

DEUTERATED FORMS OF AMINOSTEROLS AND METHODS OF USING THE SAME

-

, (2020/08/30)

Described are deuterated forms of aminosterols, or a pharmaceutically acceptable salt thereof, wherein one or more hydrogen atoms at one or more positions selected from C1, C2, C3, C4, C5, C6, C7, C8, C9, C11, C12, C14, C15, C16, C17, C18, C19, C20, C21,

Study on the Structure Activity Relationships of NPTX-594, a Spider Toxin Belonging to the Type-B Acylpolyamine Structure

Wakamiya, Tateaki,Kinoshita, Tomohiko,Hattori, Yoshihide,Yamaguchi, Yoshihiro,Naoki, Hideo,Corzo, Gerardo,Nakajimal, Terumi

, p. 331 - 340 (2007/10/03)

In order to elucidate the structure activity relationships of the spider toxin termed NPTX-594, eleven toxin analogs were designed and synthesized, and their paralytic activities against cricket were tested. As a result of the present study, it was clarif

Condensed-purines syntheses of tetrahydro-1,4-diazepino[1,2,3-gh]purin- 2-one and hexahydro-1,4-diazocino[1,2,3-gh]purin-2-one

Suzuki, Hirokazu,Sawanishi, Hiroyuki,Yamamoto, Kenji,Miyamoto, Ken-Ichi

, p. 1322 - 1325 (2007/10/03)

1,4-Pyrimido- (2a), 1,4-diazepino- (2b), and 1,4-diazocino[1,2,3- gh]purine (2c) were designed as selective cAMP-phosphodiesterase 4 (PDE 4) inhibitors. The desired condensed-purines (2b,c) were synthesized by reaction of 7-aminoalkyl-3-propylpurine-2,4-d

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