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886202-59-1

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886202-59-1 Usage

Uses

suzuki reaction

Check Digit Verification of cas no

The CAS Registry Mumber 886202-59-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,2,0 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 886202-59:
(8*8)+(7*8)+(6*6)+(5*2)+(4*0)+(3*2)+(2*5)+(1*9)=191
191 % 10 = 1
So 886202-59-1 is a valid CAS Registry Number.

886202-59-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name D-Alanine, N-(1-oxooctadecyl)-

1.2 Other means of identification

Product number -
Other names N-Octadecanoyl-D-alanine

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:886202-59-1 SDS

886202-59-1Upstream product

886202-59-1Downstream Products

886202-59-1Relevant articles and documents

Self-assembled helical ribbon and tubes of alanine-based amphiphiles induced by two different formation mechanisms

Lee, Soo Jin,Kim, Eunjeong,Seo, Moo Lyong,Do, Youngkyu,Lee, Young-A.,Lee, Shim Sung,Jung, Jong Hwa,Kogiso, Masaki,Shimizu, Toshimi

, p. 1301 - 1308 (2008)

Three long chain alanine-based amphiphiles (1-3) possessing either a saturated long alkyl chain group or unsaturated groups as the self-assembling unit of a highly organized molecular architecture were synthesized. Their self-assembling properties were investigated using EF-TEM, SEM, CD, XRD, and FTIR. The d-form (1) and the l-form (2) enantiomers showed the opposite CD signals. Furthermore, electron micrographs of the self-assembled 1 and 2 exhibited right- and left-handed helical structures, respectively. The helical structures of amphiphiles 1 and 2 were developed into tubular structures by slow cooling. On the other hand, in the helical ribbon growth process, the helical pitch and ribbon width were changed in fast cooling process. The findings strongly imply that the helical ribbon growth of alanine-based amphiphiles can be induced by two different pathways. This mechanism, quite different from that observed for sugar- and cholesterol-based tubes, is a rare example for a tube formation process.

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