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136315-70-3

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  • Cyclopentanecarboxylicacid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, (1R,2S)-rel- Manufacturer/High quality/Best price/In stock

    Cas No: 136315-70-3

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136315-70-3 Usage

Chemical Properties

white to almost white fine crystalline powder

Uses

cis-2-(tert-Butoxycarbonylamino)-1-cyclopentanecarboxylic acid is carboxylic acid derivatives and can be used as a pharmaceutical intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 136315-70-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,3,1 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 136315-70:
(8*1)+(7*3)+(6*6)+(5*3)+(4*1)+(3*5)+(2*7)+(1*0)=113
113 % 10 = 3
So 136315-70-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H19NO4/c1-11(2,3)16-10(15)12-8-6-4-5-7(8)9(13)14/h7-8H,4-6H2,1-3H3,(H,12,15)(H,13,14)/t7-,8+/m1/s1

136315-70-3 Well-known Company Product Price

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  • Aldrich

  • (713856)  (±)-cis-2-(Boc-amino)cyclopentanecarboxylicacid  ≥97.0%

  • 136315-70-3

  • 713856-500MG

  • 1,274.13CNY

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136315-70-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name cis-2-(tert-Butoxycarbonylamino)-1-cyclopentanecarboxylic acid

1.2 Other means of identification

Product number -
Other names (1R,2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]cyclopentane-1-carboxylic acid

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:136315-70-3 SDS

136315-70-3Relevant articles and documents

Amipurimycin: Total Synthesis of the Proposed Structures and Diastereoisomers

Wang, Shengyang,Sun, Jiansong,Zhang, Qingju,Cao, Xin,Zhao, Yachen,Tang, Gongli,Yu, Biao

supporting information, p. 2884 - 2888 (2018/02/16)

The proposed diastereoisomers (1 a–d) together with their C8′-epimers (1 e–h) of amipurimycin, a unique antifungal peptidyl nucleoside antibiotic, have been synthesized for the first time. The synthetic approach is efficient and stereodivergent, and features a stereoselective aldol condensation to build the branched C9 sugar amino acid skeleton and a regio- and stereocontrolled gold(I)-catalyzed N-glycosylation to furnish the purine nucleoside. Analysis of the NMR data suggests that the previously assigned configuration of the tertiary C3′ in amipurimycin should be of opposite configuration.

A concise synthesis of rigidified β-amino acids via sulfanyl radical addition-cyclization of oxime ethers and hydrazones

Miyata, Okiko,Muroya, Kanami,Koide, Junko,Naito, Takeaki

, p. 271 - 272 (2007/10/03)

A new route to the rigidified cyclic β-amino acids such as cispentacin has been developed by sulfanyl radical addition-cyclization of the alkenyl-tethered-oxime ethers and hydrazones.

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