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Carbamic acid, [[[(1,1-dimethylethoxy)carbonyl]amino]iminomethyl]-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

194985-14-3

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194985-14-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 194985-14-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,9,8 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 194985-14:
(8*1)+(7*9)+(6*4)+(5*9)+(4*8)+(3*5)+(2*1)+(1*4)=193
193 % 10 = 3
So 194985-14-3 is a valid CAS Registry Number.

194985-14-3SDS

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 N1-(benzyloxycarbonyl)-N2-(tert-butoxycarbonyl)guanidine

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:194985-14-3 SDS

194985-14-3Relevant academic research and scientific papers

Ng-acylated imidazolylpropylguanidines as potent histamine H4 receptor agonists: selectivity by variation of the n g-substituent?

Igel, Patrick,Schneider, Erich,Schnell, David,Elz, Sigurd,Seifert, Roland,Buschauer, Armin

supporting information; experimental part, p. 2623 - 2627 (2010/03/24)

3-(1H-Imidazol-4-yl)propylguanidine (SK&F 91486, 4) was identified as a potent partial agonist at the human histamine H3 receptor (hH3R) and human histamine H4 receptor (hH4R). With the aim to increase selectivity for the

Palladium- or iridium-catalyzed allylic substitution of guanidines: Convenient and direct modification of guanidines

Miyabe, Hideto,Yoshida, Kazumasa,Reddy, Valluru Krishna,Takemoto, Yoshiji

supporting information; experimental part, p. 305 - 311 (2009/04/07)

(Chemical Equation Presented) As a convenient and direct functionalization of guanidines, the transition metal-catalyzed allylic substitution of guanidines was studied. The guanidine derivatives bearing two electron-withdrawing substituents acted as react

Serine protease inhibitors

-

, (2008/06/13)

PCT No. PCT/EP97/00625 Sec. 371 Date Aug. 12, 1998 Sec. 102(e) Date Aug. 12, 1998 PCT Filed Feb. 11, 1997 PCT Pub. No. WO97/30073 PCT Pub. Date Aug. 21, 1997The invention relates to a compound having formula (I), wherein A, B, X, N, Z and Q are defined as

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