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35909-93-4

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35909-93-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35909-93-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,9,0 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 35909-93:
(7*3)+(6*5)+(5*9)+(4*0)+(3*9)+(2*9)+(1*3)=144
144 % 10 = 4
So 35909-93-4 is a valid CAS Registry Number.

35909-93-4SDS

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 Cbz-aspartic acid α,β-dimethyl ester

1.2 Other means of identification

Product number -
Other names dimethyl (S)-N-(benzyloxycarbonyl)aspartate

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:35909-93-4 SDS

35909-93-4Relevant articles and documents

Enzymatic Synthesis and Stereocomplex Formation of Chiral Polyester Containing Long-Chain Aliphatic Alcohol Backbone

Xia, Bo,Zhang, Yu,Zhu, Qiaoyan,Lin, Xianfu,Wu, Qi

, p. 3584 - 3591 (2019)

Herein we demonstrated a novel lipase-catalyzed synthesis of isotactic D-/L-poly(aspartate-octanediol) ester containing long chain alcohols backbone and discovered their stereocomplex feature with an increased Tm for the first time. Simple desi

Silyl Group-Directed 6-exo-dig Iodocyclization of Homopropargylic Carbamates and Amides

Okitsu, Takashi,Nakahigashi, Hikaru,Sugihara, Ryosuke,Fukuda, Ikki,Tsuji, Saki,In, Yasuko,Wada, Akimori

, p. 18638 - 18642 (2018/12/04)

Iodocyclization of silyl group-substituted homopropargylic carbamates and amides proceeded via 6-exo-dig mode to afford 6-vinylene-4,5-dihydro-1,3-oxazines in moderate to quantitative yields. This is the first report for silyl group-solely directed iodocy

A direct route to 2,2,5-trisubstituted pyrrolidines of relevance to kaitocephalin

Chandan, Nandkishkor,Moloney, Mark G.

supporting information, p. 1987 - 1990 (2013/04/10)

2,2,5-Trisubstituted pyrrolidines of relevance to the core of kaitocephalin are readily available by an oxime ring closure using substrates derived from aspartic acid.

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